Nanopublications

Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }

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NP93912.RAmGn5L2KH8lTL6QkfcHrFrbBcnG5Cl6OJ_lCJQpy4LqQ130_assertion description "[Framingham 100K SNP data is a resource for association tests of known and novel genes with diabetes and related traits posted at http://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?id=phs000007 webcite. Framingham 100K data replicate the TCF7L2 association with diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93912.RAmGn5L2KH8lTL6QkfcHrFrbBcnG5Cl6OJ_lCJQpy4LqQ130_provenance.
NP93913.RAnlKNXB0wEq2JSTFx6A4AB919k4vS69zUBw3W6dos2iU130_assertion description "[Framingham 100K SNP data is a resource for association tests of known and novel genes with diabetes and related traits posted at http://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?id=phs000007 webcite. Framingham 100K data replicate the TCF7L2 association with diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93913.RAnlKNXB0wEq2JSTFx6A4AB919k4vS69zUBw3W6dos2iU130_provenance.
NP93920.RAltBxXX2t2QeM0_RUCD083_bcUnUoCwAcZTBUK18DFdY130_assertion description "[The results from this GWAS generate hypotheses regarding several SNPs that may be associated with SCA phenotypes in multiple arterial beds. Given the number of tests conducted, subsequent independent replication in a staged approach is essential to identify genetic variants that may be implicated in atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93920.RAltBxXX2t2QeM0_RUCD083_bcUnUoCwAcZTBUK18DFdY130_provenance.
NP93927.RArX_1nvyAu5-xKIDbeLRRpntT9ndjKO2je0S3xnQZn8o130_assertion description "[The results from this GWAS generate hypotheses regarding several SNPs that may be associated with SCA phenotypes in multiple arterial beds. Given the number of tests conducted, subsequent independent replication in a staged approach is essential to identify genetic variants that may be implicated in atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93927.RArX_1nvyAu5-xKIDbeLRRpntT9ndjKO2je0S3xnQZn8o130_provenance.
NP93933.RAjnWRdb9yi9PI2rxs3jznk_QM17jj3HbolvGEK1ZS_kQ130_assertion description "[The results from this GWAS generate hypotheses regarding several SNPs that may be associated with SCA phenotypes in multiple arterial beds. Given the number of tests conducted, subsequent independent replication in a staged approach is essential to identify genetic variants that may be implicated in atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93933.RAjnWRdb9yi9PI2rxs3jznk_QM17jj3HbolvGEK1ZS_kQ130_provenance.
NP93936.RAn3VZcktooymZToKJiqlnGJY3RudY7T9xAL2dtQ5o_70130_assertion description "[The results from this GWAS generate hypotheses regarding several SNPs that may be associated with SCA phenotypes in multiple arterial beds. Given the number of tests conducted, subsequent independent replication in a staged approach is essential to identify genetic variants that may be implicated in atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93936.RAn3VZcktooymZToKJiqlnGJY3RudY7T9xAL2dtQ5o_70130_provenance.
NP93942.RAvK9JoXPjMkVJhZymgKjlM7Clyl7d87z2RCPgiwWH-RI130_assertion description "[The results from this GWAS generate hypotheses regarding several SNPs that may be associated with SCA phenotypes in multiple arterial beds. Given the number of tests conducted, subsequent independent replication in a staged approach is essential to identify genetic variants that may be implicated in atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93942.RAvK9JoXPjMkVJhZymgKjlM7Clyl7d87z2RCPgiwWH-RI130_provenance.
NP93943.RAuVArbFlYFSv6WKy3rNV7xODR1RY_ZyhROP3-cSumO8Q130_assertion description "[The results from this GWAS generate hypotheses regarding several SNPs that may be associated with SCA phenotypes in multiple arterial beds. Given the number of tests conducted, subsequent independent replication in a staged approach is essential to identify genetic variants that may be implicated in atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93943.RAuVArbFlYFSv6WKy3rNV7xODR1RY_ZyhROP3-cSumO8Q130_provenance.
NP93946.RAhRCioFlBrW1joE-sM-vJO6ROzpUqx1ylZp-DFLYB8bg130_assertion description "[The results from this GWAS generate hypotheses regarding several SNPs that may be associated with SCA phenotypes in multiple arterial beds. Given the number of tests conducted, subsequent independent replication in a staged approach is essential to identify genetic variants that may be implicated in atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93946.RAhRCioFlBrW1joE-sM-vJO6ROzpUqx1ylZp-DFLYB8bg130_provenance.
NP93963.RAjGwhGz1nLGZyi3l1Gupu2hE3_Od9WYzcWTiuB--70bs130_assertion description "[The results from this GWAS generate hypotheses regarding several SNPs that may be associated with SCA phenotypes in multiple arterial beds. Given the number of tests conducted, subsequent independent replication in a staged approach is essential to identify genetic variants that may be implicated in atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93963.RAjGwhGz1nLGZyi3l1Gupu2hE3_Od9WYzcWTiuB--70bs130_provenance.
NP93964.RAnHXMRMLJDP2KwH4RRWfFggzafDpvhhYrAm-wISYwj38130_assertion description "[The results from this GWAS generate hypotheses regarding several SNPs that may be associated with SCA phenotypes in multiple arterial beds. Given the number of tests conducted, subsequent independent replication in a staged approach is essential to identify genetic variants that may be implicated in atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93964.RAnHXMRMLJDP2KwH4RRWfFggzafDpvhhYrAm-wISYwj38130_provenance.
NP93966.RAoeK0ap97nWUUD7cwWZ5vTvWMwyq32LLVS2jN7mDreqU130_assertion description "[The results from this GWAS generate hypotheses regarding several SNPs that may be associated with SCA phenotypes in multiple arterial beds. Given the number of tests conducted, subsequent independent replication in a staged approach is essential to identify genetic variants that may be implicated in atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93966.RAoeK0ap97nWUUD7cwWZ5vTvWMwyq32LLVS2jN7mDreqU130_provenance.
NP93970.RApjrjR2HQBgbo5auFXdlKi44tB-Jhp6CVVHFaXtJfOuY130_assertion description "[The results from this GWAS generate hypotheses regarding several SNPs that may be associated with SCA phenotypes in multiple arterial beds. Given the number of tests conducted, subsequent independent replication in a staged approach is essential to identify genetic variants that may be implicated in atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93970.RApjrjR2HQBgbo5auFXdlKi44tB-Jhp6CVVHFaXtJfOuY130_provenance.
NP93973.RAlluJj3ffazeTEjQvs6tl9mJEPD8aoQTE8RFd91XuypA130_assertion description "[The results from this GWAS generate hypotheses regarding several SNPs that may be associated with SCA phenotypes in multiple arterial beds. Given the number of tests conducted, subsequent independent replication in a staged approach is essential to identify genetic variants that may be implicated in atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93973.RAlluJj3ffazeTEjQvs6tl9mJEPD8aoQTE8RFd91XuypA130_provenance.
NP93975.RAkEMYxmWP0oCAi5svB4HFw7jxAdcZQePSF8ENnGlhx-I130_assertion description "[The results from this GWAS generate hypotheses regarding several SNPs that may be associated with SCA phenotypes in multiple arterial beds. Given the number of tests conducted, subsequent independent replication in a staged approach is essential to identify genetic variants that may be implicated in atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93975.RAkEMYxmWP0oCAi5svB4HFw7jxAdcZQePSF8ENnGlhx-I130_provenance.
NP93978.RAvrBpXao6eGZU_NhhweZ3na4R30CVp6UD5Up7Xogsm2E130_assertion description "[The results from this GWAS generate hypotheses regarding several SNPs that may be associated with SCA phenotypes in multiple arterial beds. Given the number of tests conducted, subsequent independent replication in a staged approach is essential to identify genetic variants that may be implicated in atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93978.RAvrBpXao6eGZU_NhhweZ3na4R30CVp6UD5Up7Xogsm2E130_provenance.
NP93981.RAt6Jc4LyewMybEXmit1XDzQICIllI56B3m-O6N1qacCw130_assertion description "[The results from this GWAS generate hypotheses regarding several SNPs that may be associated with SCA phenotypes in multiple arterial beds. Given the number of tests conducted, subsequent independent replication in a staged approach is essential to identify genetic variants that may be implicated in atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93981.RAt6Jc4LyewMybEXmit1XDzQICIllI56B3m-O6N1qacCw130_provenance.
NP93983.RAhciD52kun6EerMn4Q3DsBqMKdkWBvFHfd6_n5T1rR6w130_assertion description "[The results from this GWAS generate hypotheses regarding several SNPs that may be associated with SCA phenotypes in multiple arterial beds. Given the number of tests conducted, subsequent independent replication in a staged approach is essential to identify genetic variants that may be implicated in atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93983.RAhciD52kun6EerMn4Q3DsBqMKdkWBvFHfd6_n5T1rR6w130_provenance.
NP93986.RArN2p9CHsLzoEOImaP-vPrgrFrHVbYgLKqeaH_bWQHBE130_assertion description "[The results from this GWAS generate hypotheses regarding several SNPs that may be associated with SCA phenotypes in multiple arterial beds. Given the number of tests conducted, subsequent independent replication in a staged approach is essential to identify genetic variants that may be implicated in atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93986.RArN2p9CHsLzoEOImaP-vPrgrFrHVbYgLKqeaH_bWQHBE130_provenance.
NP93989.RAqWTVKTOzPPyoyVbItUIHg3koM7O9kcdPLaJXfCTMpg0130_assertion description "[The results from this GWAS generate hypotheses regarding several SNPs that may be associated with SCA phenotypes in multiple arterial beds. Given the number of tests conducted, subsequent independent replication in a staged approach is essential to identify genetic variants that may be implicated in atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93989.RAqWTVKTOzPPyoyVbItUIHg3koM7O9kcdPLaJXfCTMpg0130_provenance.
NP93990.RAupD7bR8nAt1ds9ly-35BrpkKFkZTDpYQJZnltQOp94s130_assertion description "[The results from this GWAS generate hypotheses regarding several SNPs that may be associated with SCA phenotypes in multiple arterial beds. Given the number of tests conducted, subsequent independent replication in a staged approach is essential to identify genetic variants that may be implicated in atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93990.RAupD7bR8nAt1ds9ly-35BrpkKFkZTDpYQJZnltQOp94s130_provenance.
NP93991.RAmVsj-EAHROE5zzHho4_S6_Z8Gu0G40j0FhdiI_vSDIM130_assertion description "[The results from this GWAS generate hypotheses regarding several SNPs that may be associated with SCA phenotypes in multiple arterial beds. Given the number of tests conducted, subsequent independent replication in a staged approach is essential to identify genetic variants that may be implicated in atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93991.RAmVsj-EAHROE5zzHho4_S6_Z8Gu0G40j0FhdiI_vSDIM130_provenance.
NP93992.RAicCZQ95v4fJJwuyqx1XkW5p8vvNz2e2HucL74voEOCg130_assertion description "[The results from this GWAS generate hypotheses regarding several SNPs that may be associated with SCA phenotypes in multiple arterial beds. Given the number of tests conducted, subsequent independent replication in a staged approach is essential to identify genetic variants that may be implicated in atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93992.RAicCZQ95v4fJJwuyqx1XkW5p8vvNz2e2HucL74voEOCg130_provenance.
NP93994.RArmVj0efnD1DtXfqUX5Mmgtbsq72E7V3nwHHEBVF7s64130_assertion description "[The results from this GWAS generate hypotheses regarding several SNPs that may be associated with SCA phenotypes in multiple arterial beds. Given the number of tests conducted, subsequent independent replication in a staged approach is essential to identify genetic variants that may be implicated in atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93994.RArmVj0efnD1DtXfqUX5Mmgtbsq72E7V3nwHHEBVF7s64130_provenance.
NP93995.RAtdErTh3OTJSPOJCDubLksoDlREIEUMCHY5weyxyZXz4130_assertion description "[The results from this GWAS generate hypotheses regarding several SNPs that may be associated with SCA phenotypes in multiple arterial beds. Given the number of tests conducted, subsequent independent replication in a staged approach is essential to identify genetic variants that may be implicated in atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93995.RAtdErTh3OTJSPOJCDubLksoDlREIEUMCHY5weyxyZXz4130_provenance.
NP93996.RAifsAK_D2nZPj-Ka8lKHLp37jtnKs9pC4dMn9-cr84YA130_assertion description "[The results from this GWAS generate hypotheses regarding several SNPs that may be associated with SCA phenotypes in multiple arterial beds. Given the number of tests conducted, subsequent independent replication in a staged approach is essential to identify genetic variants that may be implicated in atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93996.RAifsAK_D2nZPj-Ka8lKHLp37jtnKs9pC4dMn9-cr84YA130_provenance.
NP93998.RAiJWgLLTCZTRVzUNCamsslp7a8aAOJ8NdJL--XeHjWyQ130_assertion description "[The results from this GWAS generate hypotheses regarding several SNPs that may be associated with SCA phenotypes in multiple arterial beds. Given the number of tests conducted, subsequent independent replication in a staged approach is essential to identify genetic variants that may be implicated in atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93998.RAiJWgLLTCZTRVzUNCamsslp7a8aAOJ8NdJL--XeHjWyQ130_provenance.
NP93999.RAoM5ait0JjgmUDYAXaSmh58jSYYiu96m9pSC_a1Qw3BQ130_assertion description "[The results from this GWAS generate hypotheses regarding several SNPs that may be associated with SCA phenotypes in multiple arterial beds. Given the number of tests conducted, subsequent independent replication in a staged approach is essential to identify genetic variants that may be implicated in atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93999.RAoM5ait0JjgmUDYAXaSmh58jSYYiu96m9pSC_a1Qw3BQ130_provenance.
NP94008.RAhv-VqJRe9vj4qDN4kfTa6p0rAiVgz2H5bY7iRdjPGR8130_assertion description "[The results from this GWAS generate hypotheses regarding several SNPs that may be associated with SCA phenotypes in multiple arterial beds. Given the number of tests conducted, subsequent independent replication in a staged approach is essential to identify genetic variants that may be implicated in atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94008.RAhv-VqJRe9vj4qDN4kfTa6p0rAiVgz2H5bY7iRdjPGR8130_provenance.
NP94016.RAv4Mt8Rb11Qsn73zOxfDMEIg88b1-WKkoXJQrNcOkR8E130_assertion description "[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated with CVD may point to novel disease pathways and identify potential targeted preventive therapies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94016.RAv4Mt8Rb11Qsn73zOxfDMEIg88b1-WKkoXJQrNcOkR8E130_provenance.
NP94023.RApPlQjfJvzq6pY-fnTakSQZ4tOWP0VtvHJV6lqhan7xU130_assertion description "[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated with CVD may point to novel disease pathways and identify potential targeted preventive therapies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94023.RApPlQjfJvzq6pY-fnTakSQZ4tOWP0VtvHJV6lqhan7xU130_provenance.
NP94024.RAg6slyPmQHY9GFICDILQGXcbQv8w1Yo9PZcGDkbpgHWs130_assertion description "[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated with CVD may point to novel disease pathways and identify potential targeted preventive therapies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94024.RAg6slyPmQHY9GFICDILQGXcbQv8w1Yo9PZcGDkbpgHWs130_provenance.
NP94029.RAuvuV3wlyVNnuvPyCa-lT8jBL-eMbgc3-g1wnilsyqO0130_assertion description "[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated with CVD may point to novel disease pathways and identify potential targeted preventive therapies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94029.RAuvuV3wlyVNnuvPyCa-lT8jBL-eMbgc3-g1wnilsyqO0130_provenance.
NP94032.RAlJbbTYOLfRkyIWOZJl_zPoJ2fPnaJukJsc49iO-zHJ4130_assertion description "[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated with CVD may point to novel disease pathways and identify potential targeted preventive therapies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94032.RAlJbbTYOLfRkyIWOZJl_zPoJ2fPnaJukJsc49iO-zHJ4130_provenance.
NP94035.RAitrwf3n4ZXnrTjl91It_twbsNMCzklnJ5Zu5zR68SFs130_assertion description "[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated with CVD may point to novel disease pathways and identify potential targeted preventive therapies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94035.RAitrwf3n4ZXnrTjl91It_twbsNMCzklnJ5Zu5zR68SFs130_provenance.
NP94039.RAhxXT0Z2JMiBt90aF8pyXtQdbZLumu5vAtcMy4CEqCDY130_assertion description "[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated with CVD may point to novel disease pathways and identify potential targeted preventive therapies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94039.RAhxXT0Z2JMiBt90aF8pyXtQdbZLumu5vAtcMy4CEqCDY130_provenance.
NP94043.RAhNHS9n8ncOkCUiAAv00CmTnLPEmkiJSr6Vr5Ncws9Ak130_assertion description "[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated with CVD may point to novel disease pathways and identify potential targeted preventive therapies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94043.RAhNHS9n8ncOkCUiAAv00CmTnLPEmkiJSr6Vr5Ncws9Ak130_provenance.
NP94044.RAqMKW1hchwRGoK5xHSj-ElZdAoUQ8dLBtjxwWE39nEKE130_assertion description "[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated with CVD may point to novel disease pathways and identify potential targeted preventive therapies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94044.RAqMKW1hchwRGoK5xHSj-ElZdAoUQ8dLBtjxwWE39nEKE130_provenance.
NP94045.RAtTw_swIx6S45pLd9aUXuF3RP2m3FTPc1_kBxGavw4z0130_assertion description "[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated with CVD may point to novel disease pathways and identify potential targeted preventive therapies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94045.RAtTw_swIx6S45pLd9aUXuF3RP2m3FTPc1_kBxGavw4z0130_provenance.
NP94053.RAjzFm32SnnQ0r1PV-7veesgm_oAWtMv_RTg5qH-V0IXc130_assertion description "[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated with CVD may point to novel disease pathways and identify potential targeted preventive therapies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94053.RAjzFm32SnnQ0r1PV-7veesgm_oAWtMv_RTg5qH-V0IXc130_provenance.
NP94066.RAjBPF2TaAsxnNWhpF-w479B2UAPYYi6kiAoNnfFdtL0M130_assertion description "[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated with CVD may point to novel disease pathways and identify potential targeted preventive therapies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94066.RAjBPF2TaAsxnNWhpF-w479B2UAPYYi6kiAoNnfFdtL0M130_provenance.
NP94067.RApuGC_tBbNT4djk1me9R8Vhg0IXSJFUB-g7NrDP8IQFw130_assertion description "[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated with CVD may point to novel disease pathways and identify potential targeted preventive therapies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94067.RApuGC_tBbNT4djk1me9R8Vhg0IXSJFUB-g7NrDP8IQFw130_provenance.
NP94074.RAl1xW4j3DvI_4W8V6px9G7tJ195K0xCtGqknbiyZcjY4130_assertion description "[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated with CVD may point to novel disease pathways and identify potential targeted preventive therapies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94074.RAl1xW4j3DvI_4W8V6px9G7tJ195K0xCtGqknbiyZcjY4130_provenance.
NP94081.RAqaFCXHQdlfjClEWHa8SSSa5IDr3vTpcSsWvP55J_F9s130_assertion description "[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated with CVD may point to novel disease pathways and identify potential targeted preventive therapies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94081.RAqaFCXHQdlfjClEWHa8SSSa5IDr3vTpcSsWvP55J_F9s130_provenance.
NP94083.RAnfBKkoBn5JrnTB0WMOyMJ_VyWYagbyrn6lHCfjtGhhg130_assertion description "[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated with CVD may point to novel disease pathways and identify potential targeted preventive therapies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94083.RAnfBKkoBn5JrnTB0WMOyMJ_VyWYagbyrn6lHCfjtGhhg130_provenance.
NP94086.RAklVBnLd_KEe1Z0AQ2XA5f3s53TUeQd1Px9zgoj56fHI130_assertion description "[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated with CVD may point to novel disease pathways and identify potential targeted preventive therapies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94086.RAklVBnLd_KEe1Z0AQ2XA5f3s53TUeQd1Px9zgoj56fHI130_provenance.
NP94090.RApNFtsXb0q6oI8ks6uqZ0gLJTrKplpFSqj_NQ_ghs-pk130_assertion description "[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated with CVD may point to novel disease pathways and identify potential targeted preventive therapies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94090.RApNFtsXb0q6oI8ks6uqZ0gLJTrKplpFSqj_NQ_ghs-pk130_provenance.
NP94091.RAgj5ekehLcpL0BX5XJShP1xJ_LfpvyhDZ4Zs-i0WOxmM130_assertion description "[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated with CVD may point to novel disease pathways and identify potential targeted preventive therapies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94091.RAgj5ekehLcpL0BX5XJShP1xJ_LfpvyhDZ4Zs-i0WOxmM130_provenance.
NP94097.RAvHbBzLNH7Vsn8CH2c8d5xHmNNWpIdixIC4w8GmI7z7s130_assertion description "[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated with CVD may point to novel disease pathways and identify potential targeted preventive therapies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94097.RAvHbBzLNH7Vsn8CH2c8d5xHmNNWpIdixIC4w8GmI7z7s130_provenance.
NP94098.RAriT13JBcmS0nUs08RWhnutPfJ2W4bSDfxivBPkagJLY130_assertion description "[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated with CVD may point to novel disease pathways and identify potential targeted preventive therapies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94098.RAriT13JBcmS0nUs08RWhnutPfJ2W4bSDfxivBPkagJLY130_provenance.
NP94110.RAuzaoBTyJPqcoV3kNaizrYpX-AIz9k5KJscTHvaFnDpI130_assertion description "[Although no association attained genome-wide significance, several interesting associations emerged for breast and prostate cancer. These findings can serve as a resource for replication in other populations to identify novel biologic pathways contributing to cancer susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94110.RAuzaoBTyJPqcoV3kNaizrYpX-AIz9k5KJscTHvaFnDpI130_provenance.
NP94111.RAimQWMZUQ7kmWiVGWQBcFm9nCnnQcQ8FKc7WhjpAibJA130_assertion description "[Although no association attained genome-wide significance, several interesting associations emerged for breast and prostate cancer. These findings can serve as a resource for replication in other populations to identify novel biologic pathways contributing to cancer susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94111.RAimQWMZUQ7kmWiVGWQBcFm9nCnnQcQ8FKc7WhjpAibJA130_provenance.
NP94114.RAknPLKsqbkK0QieOdeW6IU7bICQHSUMsnWe9hhr9kS38130_assertion description "[Although no association attained genome-wide significance, several interesting associations emerged for breast and prostate cancer. These findings can serve as a resource for replication in other populations to identify novel biologic pathways contributing to cancer susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94114.RAknPLKsqbkK0QieOdeW6IU7bICQHSUMsnWe9hhr9kS38130_provenance.
NP94116.RAqy0UxIigU0b8vKaQUZgUBBu64yXRgSgIR5sipU8cowk130_assertion description "[Although no association attained genome-wide significance, several interesting associations emerged for breast and prostate cancer. These findings can serve as a resource for replication in other populations to identify novel biologic pathways contributing to cancer susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94116.RAqy0UxIigU0b8vKaQUZgUBBu64yXRgSgIR5sipU8cowk130_provenance.
NP94118.RAizXLE1Ll-vqncK1YVfmNPboOFAGyXQDgWMoxGcW8QWQ130_assertion description "[Although no association attained genome-wide significance, several interesting associations emerged for breast and prostate cancer. These findings can serve as a resource for replication in other populations to identify novel biologic pathways contributing to cancer susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94118.RAizXLE1Ll-vqncK1YVfmNPboOFAGyXQDgWMoxGcW8QWQ130_provenance.
NP94121.RAvkgp5KqD2Ftm6lLP3G2wfVQi3BSTxe2Niyn7D2AyyRE130_assertion description "[Although no association attained genome-wide significance, several interesting associations emerged for breast and prostate cancer. These findings can serve as a resource for replication in other populations to identify novel biologic pathways contributing to cancer susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94121.RAvkgp5KqD2Ftm6lLP3G2wfVQi3BSTxe2Niyn7D2AyyRE130_provenance.
NP94122.RAiGVaoQslWxGOCH_Rwi5iOqaRNgRKeMgm7TK_jleMn-E130_assertion description "[Although no association attained genome-wide significance, several interesting associations emerged for breast and prostate cancer. These findings can serve as a resource for replication in other populations to identify novel biologic pathways contributing to cancer susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94122.RAiGVaoQslWxGOCH_Rwi5iOqaRNgRKeMgm7TK_jleMn-E130_provenance.
NP94124.RAnAmZ7nqJXx4-WKLiYgtm3hBOGNsqfU3uorlIiZvMqZE130_assertion description "[Although no association attained genome-wide significance, several interesting associations emerged for breast and prostate cancer. These findings can serve as a resource for replication in other populations to identify novel biologic pathways contributing to cancer susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94124.RAnAmZ7nqJXx4-WKLiYgtm3hBOGNsqfU3uorlIiZvMqZE130_provenance.
NP94125.RAjcdI7WAT0t8YtK8HyO1dqgG4qY4mC5v0nRHIV0gN4Y0130_assertion description "[Although no association attained genome-wide significance, several interesting associations emerged for breast and prostate cancer. These findings can serve as a resource for replication in other populations to identify novel biologic pathways contributing to cancer susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94125.RAjcdI7WAT0t8YtK8HyO1dqgG4qY4mC5v0nRHIV0gN4Y0130_provenance.
NP94129.RAhLnxJoaJ3uqxUSQ2t5H01NKKlhYxlCYJxTI9EMrmdfs130_assertion description "[Although no association attained genome-wide significance, several interesting associations emerged for breast and prostate cancer. These findings can serve as a resource for replication in other populations to identify novel biologic pathways contributing to cancer susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94129.RAhLnxJoaJ3uqxUSQ2t5H01NKKlhYxlCYJxTI9EMrmdfs130_provenance.
NP94133.RAkvvt-JT5eIFj6e6Zit3pKqFvJeiF37WR0PyGyfKpGUE130_assertion description "[Although no association attained genome-wide significance, several interesting associations emerged for breast and prostate cancer. These findings can serve as a resource for replication in other populations to identify novel biologic pathways contributing to cancer susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94133.RAkvvt-JT5eIFj6e6Zit3pKqFvJeiF37WR0PyGyfKpGUE130_provenance.
NP94139.RAlBEghAsN6wNGH_NX3QZ5dJOVG36803ezi0H2_DH1U-4130_assertion description "[This analysis confirms prior reports of significant heritability of sleepiness, usual bedtime, and usual sleep duration. Several genetic loci with suggestive linkage to these traits are identified, including linkage peaks containing circadian clock-related genes. Association tests identify NPSR1 and PDE4D as possible mediators of bedtime and sleepiness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94139.RAlBEghAsN6wNGH_NX3QZ5dJOVG36803ezi0H2_DH1U-4130_provenance.
NP94141.RAg8Tk87R1oAliTep-PtbDRKM-Ph70PQVlHAqqS7zFh2E130_assertion description "[This analysis confirms prior reports of significant heritability of sleepiness, usual bedtime, and usual sleep duration. Several genetic loci with suggestive linkage to these traits are identified, including linkage peaks containing circadian clock-related genes. Association tests identify NPSR1 and PDE4D as possible mediators of bedtime and sleepiness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94141.RAg8Tk87R1oAliTep-PtbDRKM-Ph70PQVlHAqqS7zFh2E130_provenance.
NP94143.RAs17Qmnu6EoOxnt7NGrVj3Kn-CWFmC93gEaam1Mp71V0130_assertion description "[This analysis confirms prior reports of significant heritability of sleepiness, usual bedtime, and usual sleep duration. Several genetic loci with suggestive linkage to these traits are identified, including linkage peaks containing circadian clock-related genes. Association tests identify NPSR1 and PDE4D as possible mediators of bedtime and sleepiness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94143.RAs17Qmnu6EoOxnt7NGrVj3Kn-CWFmC93gEaam1Mp71V0130_provenance.
NP94146.RAg8DCqYaPERZlN5LeWegMGOufjarvhQvuvPTHHu7_VTQ130_assertion description "[This analysis confirms prior reports of significant heritability of sleepiness, usual bedtime, and usual sleep duration. Several genetic loci with suggestive linkage to these traits are identified, including linkage peaks containing circadian clock-related genes. Association tests identify NPSR1 and PDE4D as possible mediators of bedtime and sleepiness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94146.RAg8DCqYaPERZlN5LeWegMGOufjarvhQvuvPTHHu7_VTQ130_provenance.
NP94158.RAoSUzBcqrJPz03TH-GCL890gpTplMd1VufCZcfK_P6GY130_assertion description "[A genome-wide association study of sporadic ALS in a homogenous Irish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94158.RAoSUzBcqrJPz03TH-GCL890gpTplMd1VufCZcfK_P6GY130_provenance.
NP94160.RAsL3C5XSzie-WrYwjUBTg7VRk9aBh-4imMrBB2iIrf2Y130_assertion description "[A genome-wide association study of sporadic ALS in a homogenous Irish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94160.RAsL3C5XSzie-WrYwjUBTg7VRk9aBh-4imMrBB2iIrf2Y130_provenance.
NP94162.RAjeIuHFbvxed1auVy4f6yaHqrIx_VH7NedTryUYp4Jv8130_assertion description "[A genome-wide association study of sporadic ALS in a homogenous Irish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94162.RAjeIuHFbvxed1auVy4f6yaHqrIx_VH7NedTryUYp4Jv8130_provenance.
NP94180.RAuf2urrM0WGn0vNm_WmZP8aAvcPAAF2RxMAfPJ-XeiUo130_assertion description "[A genome-wide association study of sporadic ALS in a homogenous Irish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94180.RAuf2urrM0WGn0vNm_WmZP8aAvcPAAF2RxMAfPJ-XeiUo130_provenance.
NP94183.RApEYNG5N5CS_4spwuPj-1af5BF1BZeilch-0q1z202yI130_assertion description "[A genome-wide association study of sporadic ALS in a homogenous Irish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94183.RApEYNG5N5CS_4spwuPj-1af5BF1BZeilch-0q1z202yI130_provenance.
NP94187.RAsPM0waBqiEUGWfi26TbMchfR8B0FeUmlnaONCjUFdkA130_assertion description "[A genome-wide association study of sporadic ALS in a homogenous Irish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94187.RAsPM0waBqiEUGWfi26TbMchfR8B0FeUmlnaONCjUFdkA130_provenance.
NP94188.RAnQKrp9C-224N0pdZMVlRo3pRXHxtM3xfBuyiiqI2ukA130_assertion description "[A genome-wide association study of sporadic ALS in a homogenous Irish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94188.RAnQKrp9C-224N0pdZMVlRo3pRXHxtM3xfBuyiiqI2ukA130_provenance.
NP94189.RAuX2XWCuYDSc6XO4fwwZKg1oYCzE4H8SR7nDPVgd87l8130_assertion description "[A genome-wide association study of sporadic ALS in a homogenous Irish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94189.RAuX2XWCuYDSc6XO4fwwZKg1oYCzE4H8SR7nDPVgd87l8130_provenance.
NP94190.RAmhkAgHyWUqipVnwnxsx0nc9mpljA8HQ_pbk5qrhcYto130_assertion description "[A genome-wide association study of sporadic ALS in a homogenous Irish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94190.RAmhkAgHyWUqipVnwnxsx0nc9mpljA8HQ_pbk5qrhcYto130_provenance.
NP94194.RAok51oKKjkf0qhWB4Bqr-ppQ9_hcsEG0w7ZSz6ixvIDU130_assertion description "[A genome-wide association study of sporadic ALS in a homogenous Irish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94194.RAok51oKKjkf0qhWB4Bqr-ppQ9_hcsEG0w7ZSz6ixvIDU130_provenance.
NP94197.RAokoqlzwzbJ17sf5CqqF9T8x7dEuGxNb9S6bL5zOp9AM130_assertion description "[A genome-wide association study of sporadic ALS in a homogenous Irish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94197.RAokoqlzwzbJ17sf5CqqF9T8x7dEuGxNb9S6bL5zOp9AM130_provenance.
NP94200.RAizrhufXX4U0OKnhCT0QaJjpdrp0oocDli-T5TBWWuhc130_assertion description "[A genome-wide association study of sporadic ALS in a homogenous Irish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94200.RAizrhufXX4U0OKnhCT0QaJjpdrp0oocDli-T5TBWWuhc130_provenance.
NP94202.RAgFmyl1O5sEvRAx_bOld109z5cJ8YLJoV4B52vi3U3iQ130_assertion description "[A genome-wide association study of sporadic ALS in a homogenous Irish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94202.RAgFmyl1O5sEvRAx_bOld109z5cJ8YLJoV4B52vi3U3iQ130_provenance.
NP94205.RAmmTIw7PkJsGg7PFhgNTJulacUe980E8TreIV2eqvliU130_assertion description "[A genome-wide association study of sporadic ALS in a homogenous Irish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94205.RAmmTIw7PkJsGg7PFhgNTJulacUe980E8TreIV2eqvliU130_provenance.
NP94206.RAgH6S_K0sB12azYwaHV9M7FhSNRg2mwtvIEi4YNDFpwQ130_assertion description "[A genome-wide association study of sporadic ALS in a homogenous Irish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94206.RAgH6S_K0sB12azYwaHV9M7FhSNRg2mwtvIEi4YNDFpwQ130_provenance.
NP94210.RAmmr8tXXkQTeWYh4Ne8tNXCgCAHdyAFYkax-vhitqOiw130_assertion description "[A genome-wide association study of sporadic ALS in a homogenous Irish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94210.RAmmr8tXXkQTeWYh4Ne8tNXCgCAHdyAFYkax-vhitqOiw130_provenance.
NP94212.RAh9uUCBbbD1F6AvKRnb3GH5D42eC3KwN9QONVn5PIg4k130_assertion description "[A genome-wide association study of sporadic ALS in a homogenous Irish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94212.RAh9uUCBbbD1F6AvKRnb3GH5D42eC3KwN9QONVn5PIg4k130_provenance.
NP94213.RAoQoz6x_REM5wWFkpysKrt3AtIWqM4YJUyWwHPjnezuc130_assertion description "[A genome-wide association study of sporadic ALS in a homogenous Irish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94213.RAoQoz6x_REM5wWFkpysKrt3AtIWqM4YJUyWwHPjnezuc130_provenance.
NP94220.RAp_y_lY3OtuVPPLgKgyP0uJTJ8_os42rtjxCd8HTzhbo130_assertion description "[A genome-wide association study of sporadic ALS in a homogenous Irish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94220.RAp_y_lY3OtuVPPLgKgyP0uJTJ8_os42rtjxCd8HTzhbo130_provenance.
NP94226.RAttT5k90rg_9HBUuqxc_YgoM57OZUQbw-2yNYxCxHnnw130_assertion description "[A genome-wide association study of sporadic ALS in a homogenous Irish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94226.RAttT5k90rg_9HBUuqxc_YgoM57OZUQbw-2yNYxCxHnnw130_provenance.
NP94236.RAn8bCaNMnqwgO6AdfI0fLkHEWZiFfuz4W60YG4gMV0G4130_assertion description "[We identified and then confirmed through replication two new genetic loci for SLE: a promoter-region allele associated with reduced expression of BLK and increased expression of C8orf13 and variants in the ITGAM-ITGAX region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94236.RAn8bCaNMnqwgO6AdfI0fLkHEWZiFfuz4W60YG4gMV0G4130_provenance.
NP94240.RAuePyvbttnt2N8NLu4mak2mTc7HjqoKdqbGYIQ6otWLQ130_assertion description "[We identified and then confirmed through replication two new genetic loci for SLE: a promoter-region allele associated with reduced expression of BLK and increased expression of C8orf13 and variants in the ITGAM-ITGAX region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94240.RAuePyvbttnt2N8NLu4mak2mTc7HjqoKdqbGYIQ6otWLQ130_provenance.
NP94242.RAiTDDDRbjjhd7omzoloeZsgYERolTPvheoCd36LKxNFM130_assertion description "[We identified and then confirmed through replication two new genetic loci for SLE: a promoter-region allele associated with reduced expression of BLK and increased expression of C8orf13 and variants in the ITGAM-ITGAX region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94242.RAiTDDDRbjjhd7omzoloeZsgYERolTPvheoCd36LKxNFM130_provenance.
NP94253.RAq3ap-Fjl6Bn0YlIaZFlQRjbVUMJJ0uU92o11_nhJ8Nk130_assertion description "[We identified and then confirmed through replication two new genetic loci for SLE: a promoter-region allele associated with reduced expression of BLK and increased expression of C8orf13 and variants in the ITGAM-ITGAX region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94253.RAq3ap-Fjl6Bn0YlIaZFlQRjbVUMJJ0uU92o11_nhJ8Nk130_provenance.
NP94255.RAj273QcLSAlplLmCg3P1zr6kY-DDMnIv58_tK_QmkSlM130_assertion description "[We identified and then confirmed through replication two new genetic loci for SLE: a promoter-region allele associated with reduced expression of BLK and increased expression of C8orf13 and variants in the ITGAM-ITGAX region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94255.RAj273QcLSAlplLmCg3P1zr6kY-DDMnIv58_tK_QmkSlM130_provenance.
NP94257.RAsZ2uvz0nsX3P9dYsaReQMe3iKLVNUOpGvfXow2yGxck130_assertion description "[We identified and then confirmed through replication two new genetic loci for SLE: a promoter-region allele associated with reduced expression of BLK and increased expression of C8orf13 and variants in the ITGAM-ITGAX region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94257.RAsZ2uvz0nsX3P9dYsaReQMe3iKLVNUOpGvfXow2yGxck130_provenance.
NP94260.RAsRP7qNqQZsH31HxYxqDt6IV6QRNNE-cUcJwamems8wM130_assertion description "[We identified and then confirmed through replication two new genetic loci for SLE: a promoter-region allele associated with reduced expression of BLK and increased expression of C8orf13 and variants in the ITGAM-ITGAX region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94260.RAsRP7qNqQZsH31HxYxqDt6IV6QRNNE-cUcJwamems8wM130_provenance.
NP94261.RAq1GXcyG9U1JjOvKfc_pEIEmwOASiE0IrNja2xK6Ea_s130_assertion description "[Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94261.RAq1GXcyG9U1JjOvKfc_pEIEmwOASiE0IrNja2xK6Ea_s130_provenance.
NP94265.RApfNDlVdUXojIqAoJwnxisbogaziIyaQOEFoG2gIZkvA130_assertion description "[Genome-wide association study identifies new prostate cancer susceptibility loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94265.RApfNDlVdUXojIqAoJwnxisbogaziIyaQOEFoG2gIZkvA130_provenance.
NP94267.RAp1Sospa4JaaCJfz954iE6-ATaSOuxh0mizLiS3ijqKc130_assertion description "[Multiple newly identified loci associated with prostate cancer susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94267.RAp1Sospa4JaaCJfz954iE6-ATaSOuxh0mizLiS3ijqKc130_provenance.
NP94268.RAgGdopXBj96w6YsDs_qVKTm8zUKMSoXDI3utALMKucgc130_assertion description "[Identification of seven new prostate cancer susceptibility loci through a genome-wide association study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94268.RAgGdopXBj96w6YsDs_qVKTm8zUKMSoXDI3utALMKucgc130_provenance.
NP94270.RAm0zSPWNPUEQPsuWQE1aHixlXRuAqOpSSZEfla1eFNZ0130_assertion description "[Genome-wide association study identifies new prostate cancer susceptibility loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94270.RAm0zSPWNPUEQPsuWQE1aHixlXRuAqOpSSZEfla1eFNZ0130_provenance.
NP94271.RAqFDdlm8HwQ2JdEGNU6KK4z5-hRKL0yRO2CJXT-vH-Hs130_assertion description "[Loci on chromosome 10 include MSMB, which encodes beta-microseminoprotein, a primary constituent of semen and a proposed prostate cancer biomarker, and CTBP2, a gene with antiapoptotic activity; the locus on chromosome 7 is at JAZF1, a transcriptional repressor that is fused by chromosome translocation to SUZ12 in endometrial cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94271.RAqFDdlm8HwQ2JdEGNU6KK4z5-hRKL0yRO2CJXT-vH-Hs130_provenance.
NP94272.RAnlIwUtuX4bk6RKE5A5Xxdtln7kUsFDNVmlq6T6rQseM130_assertion description "[Loci on chromosome 10 include MSMB, which encodes beta-microseminoprotein, a primary constituent of semen and a proposed prostate cancer biomarker, and CTBP2, a gene with antiapoptotic activity; the locus on chromosome 7 is at JAZF1, a transcriptional repressor that is fused by chromosome translocation to SUZ12 in endometrial cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94272.RAnlIwUtuX4bk6RKE5A5Xxdtln7kUsFDNVmlq6T6rQseM130_provenance.
NP94277.RAtPJs2AcZxmNqmm84BTIgL0_ArryNWQ3bBiaG119cvhE130_assertion description "[Multiple newly identified loci associated with prostate cancer susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94277.RAtPJs2AcZxmNqmm84BTIgL0_ArryNWQ3bBiaG119cvhE130_provenance.

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