Nanopublications

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

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NP94281.RAlJ3P18TS6PtVa1RgHFFOi2FXvPeNbzRilebWGd8j1TM130_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." NP94281.RAlJ3P18TS6PtVa1RgHFFOi2FXvPeNbzRilebWGd8j1TM130_provenance.
NP94282.RAvCnUM0i_8z2UPoV8YL7ZyWWQb8UEHPv4YP1M8EiearE130_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." NP94282.RAvCnUM0i_8z2UPoV8YL7ZyWWQb8UEHPv4YP1M8EiearE130_provenance.
NP94283.RAg1oPK9J2fLbeSOe2PYxnSiAjt0xnfClDwHU3yxS-Ey0130_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." NP94283.RAg1oPK9J2fLbeSOe2PYxnSiAjt0xnfClDwHU3yxS-Ey0130_provenance.
NP94285.RAmEW4v1Gj4sLBpgC-YGvNHIkir1iQVgFCLzQiNh7N2VU130_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." NP94285.RAmEW4v1Gj4sLBpgC-YGvNHIkir1iQVgFCLzQiNh7N2VU130_provenance.
NP94291.RAhkHO_J_n76ei-yAJqAkkP0dH_avp2Zk4vcsyk4L7kKg130_assertion description "[Genomewide association for schizophrenia in the CATIE study: results of stage 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94291.RAhkHO_J_n76ei-yAJqAkkP0dH_avp2Zk4vcsyk4L7kKg130_provenance.
NP94300.RAsQtZxmzEQi4521GNCneoYxs0mX7ZXEWuLPaPxsZQGpI130_assertion description "[Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94300.RAsQtZxmzEQi4521GNCneoYxs0mX7ZXEWuLPaPxsZQGpI130_provenance.
NP94301.RArk2m7L7g8B2aoVWqGmG_rPvj2l9OcvQWdqSeAbtYEaI130_assertion description "[A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94301.RArk2m7L7g8B2aoVWqGmG_rPvj2l9OcvQWdqSeAbtYEaI130_provenance.
NP94302.RAuXuHbuxyAVLUasH3tsFFRPNHQb9cY52IEyZW67ErSwI130_assertion description "[Meta-analysis of new genome-wide association studies of colorectal cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94302.RAuXuHbuxyAVLUasH3tsFFRPNHQb9cY52IEyZW67ErSwI130_provenance.
NP94303.RAuMfoXrwvlcct9qaianaaQC967Fm-q5Cosook3ldW-r4130_assertion description "[A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94303.RAuMfoXrwvlcct9qaianaaQC967Fm-q5Cosook3ldW-r4130_provenance.
NP94307.RAjeWYsZaWt_1Ao1yva42GiWC0CfC3r6vPKfVtxA35Ls0130_assertion description "[A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94307.RAjeWYsZaWt_1Ao1yva42GiWC0CfC3r6vPKfVtxA35Ls0130_provenance.
NP94312.RAmSxZl6EQ7XYdTY8VTBSxr_DBrKjUuCmi1MvXPK44e_Y130_assertion description "[A common genetic variation at chromosome band 6p22 is associated with susceptibility to neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94312.RAmSxZl6EQ7XYdTY8VTBSxr_DBrKjUuCmi1MvXPK44e_Y130_provenance.
NP94315.RAmLPOTrhI4JXxBE8xnknupnJcywrVFZ83RYXNfI59vr8130_assertion description "[A common genetic variation at chromosome band 6p22 is associated with susceptibility to neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94315.RAmLPOTrhI4JXxBE8xnknupnJcywrVFZ83RYXNfI59vr8130_provenance.
NP94322.RAvsOvBFD_5avHUzalV-VFsjOKketumkXGdbM3d0T8vqw130_assertion description "[A common genetic variation at chromosome band 6p22 is associated with susceptibility to neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94322.RAvsOvBFD_5avHUzalV-VFsjOKketumkXGdbM3d0T8vqw130_provenance.
NP94325.RAuu8MC1RNRIy6lnr6-TUeDG36yEh4gIngbqc5ZtPY_ic130_assertion description "[A common genetic variation at chromosome band 6p22 is associated with susceptibility to neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94325.RAuu8MC1RNRIy6lnr6-TUeDG36yEh4gIngbqc5ZtPY_ic130_provenance.
NP94329.RAo0VCy10lklmuF9TNT2ngJ8vEzg3GjsKg1aInwFNu_ko130_assertion description "[A common genetic variation at chromosome band 6p22 is associated with susceptibility to neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94329.RAo0VCy10lklmuF9TNT2ngJ8vEzg3GjsKg1aInwFNu_ko130_provenance.
NP94330.RAr4rN1o7Zn6Q9G0ow1UfyX5djPfJC24jnTQbQR58OnCY130_assertion description "[A common genetic variation at chromosome band 6p22 is associated with susceptibility to neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94330.RAr4rN1o7Zn6Q9G0ow1UfyX5djPfJC24jnTQbQR58OnCY130_provenance.
NP94333.RAuPuXBPY2F9TnajeyT0_XqFpiXlvLr5k-CgC0tMTyjIE130_assertion description "[A common genetic variation at chromosome band 6p22 is associated with susceptibility to neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94333.RAuPuXBPY2F9TnajeyT0_XqFpiXlvLr5k-CgC0tMTyjIE130_provenance.
NP94346.RApbcMeQH1WuMxcHxNI__JDqqEMsf3q8AjL2AT3PH69aM130_assertion description "[A common genetic variation at chromosome band 6p22 is associated with susceptibility to neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94346.RApbcMeQH1WuMxcHxNI__JDqqEMsf3q8AjL2AT3PH69aM130_provenance.
NP94348.RAgXQZ9hWwgyWU341n-hZBcDeGTcIZiJLSwBhMmY2VDXE130_assertion description "[A common genetic variation at chromosome band 6p22 is associated with susceptibility to neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94348.RAgXQZ9hWwgyWU341n-hZBcDeGTcIZiJLSwBhMmY2VDXE130_provenance.
NP94354.RArgTXb1PA5eMtVFFiXNXvcj8i7gqEeqDsbeq6_JKC0K0130_assertion description "[A common genetic variation at chromosome band 6p22 is associated with susceptibility to neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94354.RArgTXb1PA5eMtVFFiXNXvcj8i7gqEeqDsbeq6_JKC0K0130_provenance.
NP94355.RAoG3f9atVUXJ1eYNjFP9w6nDn7bAnebblRrzPlsQE7W4130_assertion description "[A common genetic variation at chromosome band 6p22 is associated with susceptibility to neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94355.RAoG3f9atVUXJ1eYNjFP9w6nDn7bAnebblRrzPlsQE7W4130_provenance.
NP94356.RAvDNVp2fNxcnoJ3pZnW0qPfEjdD_edgchIv3q_uUpLL8130_assertion description "[A common genetic variation at chromosome band 6p22 is associated with susceptibility to neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94356.RAvDNVp2fNxcnoJ3pZnW0qPfEjdD_edgchIv3q_uUpLL8130_provenance.
NP94363.RAlCW9lcdgOpFQZ99Q74VkxA1opSXxldQgmkH3Q2oXefo130_assertion description "[A common genetic variation at chromosome band 6p22 is associated with susceptibility to neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94363.RAlCW9lcdgOpFQZ99Q74VkxA1opSXxldQgmkH3Q2oXefo130_provenance.
NP94366.RAhLxL7EVu24qnjxamyn79300MrcxOXzg5qsw3oldarB8130_assertion description "[A common genetic variation at chromosome band 6p22 is associated with susceptibility to neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94366.RAhLxL7EVu24qnjxamyn79300MrcxOXzg5qsw3oldarB8130_provenance.
NP94367.RAsb2ixKyIF7fxdkIN3DCJWMmi-ngj5RQlWZv3dDk4Y0U130_assertion description "[A common genetic variation at chromosome band 6p22 is associated with susceptibility to neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94367.RAsb2ixKyIF7fxdkIN3DCJWMmi-ngj5RQlWZv3dDk4Y0U130_provenance.
NP94370.RAi9tSMoX7ae5EYZ7M6GKofFWtc_IHwPCE5t1M0kTWuEI130_assertion description "[These data show that common variation in BARD1 contributes to the etiology of the aggressive and most clinically relevant subset of human neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94370.RAi9tSMoX7ae5EYZ7M6GKofFWtc_IHwPCE5t1M0kTWuEI130_provenance.
NP94372.RAnpa4lfXXKKpmbAJDScwRLRyzdJcOduIrH4lSvXw4ayc130_assertion description "[A common genetic variation at chromosome band 6p22 is associated with susceptibility to neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94372.RAnpa4lfXXKKpmbAJDScwRLRyzdJcOduIrH4lSvXw4ayc130_provenance.
NP94374.RAnQ08vefysyDLEDbNRWNywaTJ406ARHu00s5tjVloE7o130_assertion description "[A common genetic variation at chromosome band 6p22 is associated with susceptibility to neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94374.RAnQ08vefysyDLEDbNRWNywaTJ406ARHu00s5tjVloE7o130_provenance.
NP94375.RAlm6lwL-X1LeQS__Rq72BcYnGEm5zAy3MBRZSbr2OcvY130_assertion description "[A common genetic variation at chromosome band 6p22 is associated with susceptibility to neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94375.RAlm6lwL-X1LeQS__Rq72BcYnGEm5zAy3MBRZSbr2OcvY130_provenance.
NP94378.RAkbGCQg9puA8KrWSBQ57xdOGeyMeclAuvhDvCStmH02E130_assertion description "[A common genetic variation at chromosome band 6p22 is associated with susceptibility to neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94378.RAkbGCQg9puA8KrWSBQ57xdOGeyMeclAuvhDvCStmH02E130_provenance.
NP94389.RAnMaClVNNvW-hvw7fwTtUQfKIQgKCixYqxw7uf_kR6r8130_assertion description "[Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94389.RAnMaClVNNvW-hvw7fwTtUQfKIQgKCixYqxw7uf_kR6r8130_provenance.
NP94399.RAuf_kWz3INH9f31Tal_EFShTgFTB-sjJhB6zWDMxTRUQ130_assertion description "[Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94399.RAuf_kWz3INH9f31Tal_EFShTgFTB-sjJhB6zWDMxTRUQ130_provenance.
NP94400.RAlSQbVQU8_ej6-m9xd3EGRyT8f7pHqJ60m5kzbMMrGvo130_assertion description "[A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94400.RAlSQbVQU8_ej6-m9xd3EGRyT8f7pHqJ60m5kzbMMrGvo130_provenance.
NP94406.RAt5qjm-sw03vXuXG-OWrPRbB2BNZ2-vBYX9uAbojK5k0130_assertion description "[Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in rheumatoid arthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94406.RAt5qjm-sw03vXuXG-OWrPRbB2BNZ2-vBYX9uAbojK5k0130_provenance.
NP94407.RAtgFQP1xeRCSyvHqKDb3Z_dgRSPjq6ZbxeBSLia4P_n0130_assertion description "[Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in rheumatoid arthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94407.RAtgFQP1xeRCSyvHqKDb3Z_dgRSPjq6ZbxeBSLia4P_n0130_provenance.
NP94408.RAkUaRPvA1qLVNDAvYOiSL4E7PDQPTq39QteVVo7VtvYk130_assertion description "[Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in rheumatoid arthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94408.RAkUaRPvA1qLVNDAvYOiSL4E7PDQPTq39QteVVo7VtvYk130_provenance.
NP94416.RAthEUZIRYObLpOIl0GXDgaxm0IYDrIq5aZVUfHr36ukc130_assertion description "[Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94416.RAthEUZIRYObLpOIl0GXDgaxm0IYDrIq5aZVUfHr36ukc130_provenance.
NP94417.RAgFPdTraBrH17A1ZlrMmUZyAJyOzRb8pCkDFO9O52itg130_assertion description "[Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94417.RAgFPdTraBrH17A1ZlrMmUZyAJyOzRb8pCkDFO9O52itg130_provenance.
NP94422.RAtk6ksTcZnQ3ILqDO8RbLWI-KxrmD1vZpMXdmjOd6tww130_assertion description "[An analysis of all 11,974 bipolar disorder cases and 51,792 controls confirmed genome-wide significant evidence of association for CACNA1C and identified a new intronic variant in ODZ4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94422.RAtk6ksTcZnQ3ILqDO8RbLWI-KxrmD1vZpMXdmjOd6tww130_provenance.
NP94423.RAjT69M0-N1lF2OAP-J5g8HV_kB88X3f-urX4jW6Ftb6E130_assertion description "[Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94423.RAjT69M0-N1lF2OAP-J5g8HV_kB88X3f-urX4jW6Ftb6E130_provenance.
NP94431.RAgQ4gr6FblLTSf5BQzEqGqIUdvYevgfKGh8JVXcOeOnk130_assertion description "[Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94431.RAgQ4gr6FblLTSf5BQzEqGqIUdvYevgfKGh8JVXcOeOnk130_provenance.
NP94438.RAvNwroDxWl4QjmB_fg9ZU1sjrQTn8lJyGduo1-_A3GEc130_assertion description "[A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94438.RAvNwroDxWl4QjmB_fg9ZU1sjrQTn8lJyGduo1-_A3GEc130_provenance.
NP94439.RAjLm-q6N_YcTH8GEVWbqHRDHwbk7pRQJm2vTD7MggTpk130_assertion description "[A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94439.RAjLm-q6N_YcTH8GEVWbqHRDHwbk7pRQJm2vTD7MggTpk130_provenance.
NP94443.RAiJyyGkodOIdbctn9c772behtkZdom_s5fhHtk-QGzEM130_assertion description "[The small effect sizes may limit the prognostic, diagnostic, and therapeutic use of SNP markers such as those in MAMDC1. However, the present study demonstrates the potential of a GWAS to discover potentially important pathogenic pathways for which clinically more powerful (bio)markers may eventually be developed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94443.RAiJyyGkodOIdbctn9c772behtkZdom_s5fhHtk-QGzEM130_provenance.
NP94444.RAmlEjUUZB9s0ug1jtVEW5CH9rxesACewpYszrJxKexxI130_assertion description "[The small effect sizes may limit the prognostic, diagnostic, and therapeutic use of SNP markers such as those in MAMDC1. However, the present study demonstrates the potential of a GWAS to discover potentially important pathogenic pathways for which clinically more powerful (bio)markers may eventually be developed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94444.RAmlEjUUZB9s0ug1jtVEW5CH9rxesACewpYszrJxKexxI130_provenance.
NP94446.RAog4RK5WOzI0LMbljxPspbMdT10nJbQkTTms2QzqN0DY130_assertion description "[Common variants at CD40 and other loci confer risk of rheumatoid arthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94446.RAog4RK5WOzI0LMbljxPspbMdT10nJbQkTTms2QzqN0DY130_provenance.
NP94447.RAkzUakGQqm67FZuyIVxWtmEPlR_dPSXAwnb_Gb_wtBJg130_assertion description "[Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94447.RAkzUakGQqm67FZuyIVxWtmEPlR_dPSXAwnb_Gb_wtBJg130_provenance.
NP94451.RAttXUI8Av8iaXAAjQ3bMUF325T9L82grn23SdPrsBN4o130_assertion description "[A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94451.RAttXUI8Av8iaXAAjQ3bMUF325T9L82grn23SdPrsBN4o130_provenance.
NP94458.RAsTpICw07sOeZl33Y--8L5EwwJC36jHM1jAHCHnqgudM130_assertion description "[Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94458.RAsTpICw07sOeZl33Y--8L5EwwJC36jHM1jAHCHnqgudM130_provenance.
NP94462.RAr_U80mVpldndx4OGEAljCj9BL_NNE7H56wmcNye-NB8130_assertion description "[Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94462.RAr_U80mVpldndx4OGEAljCj9BL_NNE7H56wmcNye-NB8130_provenance.
NP94463.RAnR2kA9C4XN-YGNOMSI_2H6gT5x9CEWHp-6vhBsJsiZc130_assertion description "[Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94463.RAnR2kA9C4XN-YGNOMSI_2H6gT5x9CEWHp-6vhBsJsiZc130_provenance.
NP94466.RAqii5fBl0cA0xTorZ9f4eYHt3eY8KpyiWE0KMWFfNcP4130_assertion description "[Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94466.RAqii5fBl0cA0xTorZ9f4eYHt3eY8KpyiWE0KMWFfNcP4130_provenance.
NP94477.RAjrT0Khl0xKJh-fgyolbZLCx4n9NIAf_755HJopZf4O0130_assertion description "[Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94477.RAjrT0Khl0xKJh-fgyolbZLCx4n9NIAf_755HJopZf4O0130_provenance.
NP94482.RAo7_z8Z2-cln1pN3QeiLuQ41PhQh_EMrkLkdRMcEI_ao130_assertion description "[Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94482.RAo7_z8Z2-cln1pN3QeiLuQ41PhQh_EMrkLkdRMcEI_ao130_provenance.
NP94483.RAknXRttT5fXydQriKUIOAjVJOACDONeK3YlE1lkU9ATc130_assertion description "[Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94483.RAknXRttT5fXydQriKUIOAjVJOACDONeK3YlE1lkU9ATc130_provenance.
NP94484.RAuseFq2GQSl9yVPJEDkCzagT4RVOvpYsoz7lSYIItmlw130_assertion description "[Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94484.RAuseFq2GQSl9yVPJEDkCzagT4RVOvpYsoz7lSYIItmlw130_provenance.
NP94485.RAt8sPTrWYUr3D6vP4ETSb6M4Lsrne-UYgf37U-yAzxAE130_assertion description "[Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94485.RAt8sPTrWYUr3D6vP4ETSb6M4Lsrne-UYgf37U-yAzxAE130_provenance.
NP94490.RAufmPGpQu-VGZxcxbnH85ot8v7Lp8tMoEKWTA11NwJJI130_assertion description "[Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94490.RAufmPGpQu-VGZxcxbnH85ot8v7Lp8tMoEKWTA11NwJJI130_provenance.
NP94500.RAj-On8t0F747mDjA3P2-vUMoy7TqOc2P25mPjM3LOnL8130_assertion description "[Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94500.RAj-On8t0F747mDjA3P2-vUMoy7TqOc2P25mPjM3LOnL8130_provenance.
NP94507.RAm7V_9dFAZD7aV3Gz48gTMMWwJa7VoMcHh6AOsJ51QKo130_assertion description "[Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94507.RAm7V_9dFAZD7aV3Gz48gTMMWwJa7VoMcHh6AOsJ51QKo130_provenance.
NP94510.RAjRnHV52ENDOjbRnFyDhIZeUkVjhjkzMqJ2aDmAMRkHA130_assertion description "[Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94510.RAjRnHV52ENDOjbRnFyDhIZeUkVjhjkzMqJ2aDmAMRkHA130_provenance.
NP94515.RAgJiwlhe6I5ccIHNrnoCi30jiefsdESTr2DqVL4z3-y4130_assertion description "[Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94515.RAgJiwlhe6I5ccIHNrnoCi30jiefsdESTr2DqVL4z3-y4130_provenance.
NP94516.RArtXKg8ltllQ6WJHdEbhjH37AF5NZ3pYFxDbpiNluqoc130_assertion description "[Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94516.RArtXKg8ltllQ6WJHdEbhjH37AF5NZ3pYFxDbpiNluqoc130_provenance.
NP94518.RAjCZ5W6gvAfbEeTGhjnAwspaZnMxJIZ7KJaPybIqFcrM130_assertion description "[Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94518.RAjCZ5W6gvAfbEeTGhjnAwspaZnMxJIZ7KJaPybIqFcrM130_provenance.
NP94527.RAv32-mmRen5-eFgr7cxzKbZZG5AaodKgNjeOllmvYCCs130_assertion description "[Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94527.RAv32-mmRen5-eFgr7cxzKbZZG5AaodKgNjeOllmvYCCs130_provenance.
NP94531.RAp3UUgDz37EokC5xyE11BrVSBL_NWAXbPaGU2XhHz0co130_assertion description "[Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94531.RAp3UUgDz37EokC5xyE11BrVSBL_NWAXbPaGU2XhHz0co130_provenance.
NP94535.RApJ9vo7t17vsECxtduGWWQT1g7UVphLRcHSLasGOO78A130_assertion description "[Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94535.RApJ9vo7t17vsECxtduGWWQT1g7UVphLRcHSLasGOO78A130_provenance.
NP94538.RAp0QLCe3urjnOgU6v8V0euftG9GvhPWbKVtotVsxJCXE130_assertion description "[Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94538.RAp0QLCe3urjnOgU6v8V0euftG9GvhPWbKVtotVsxJCXE130_provenance.
NP94539.RAoOeRRRJZXTfan0VgEa0b6JkXnp8jzAkZ9pL6aGdmUQ8130_assertion description "[Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94539.RAoOeRRRJZXTfan0VgEa0b6JkXnp8jzAkZ9pL6aGdmUQ8130_provenance.
NP94541.RAmtxXiQqH2D12QaKx8_Sg0i3-6PXHh6av5nCbd5fmJbI130_assertion description "[Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94541.RAmtxXiQqH2D12QaKx8_Sg0i3-6PXHh6av5nCbd5fmJbI130_provenance.
NP94544.RAo37VfCZw7xo-RwixpkGzFp76Z-6M4_V4KGJiFv7AD8k130_assertion description "[Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94544.RAo37VfCZw7xo-RwixpkGzFp76Z-6M4_V4KGJiFv7AD8k130_provenance.
NP94548.RAot5g-RCvjSiU91Wi7wxCB4U6lMGW_Mw4vg3CsTG4Ees130_assertion description "[Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94548.RAot5g-RCvjSiU91Wi7wxCB4U6lMGW_Mw4vg3CsTG4Ees130_provenance.
NP94551.RAtuJUtDHzAKNnHoCgBr-IvyZd8nOYKmbZo3oza9meApg130_assertion description "[Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94551.RAtuJUtDHzAKNnHoCgBr-IvyZd8nOYKmbZo3oza9meApg130_provenance.
NP94560.RAszbCxlUP7cOTbxZPiw8VSNbSJYsIIFaPBRL0K-X_GAc130_assertion description "[Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94560.RAszbCxlUP7cOTbxZPiw8VSNbSJYsIIFaPBRL0K-X_GAc130_provenance.
NP94565.RAqOhDMzKO_TDzhE62vXz6DXRyqw8ltLAuE_7sofuwbEY130_assertion description "[Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94565.RAqOhDMzKO_TDzhE62vXz6DXRyqw8ltLAuE_7sofuwbEY130_provenance.
NP94567.RAk_tVlLMbTug95cF3tt8muzLd_eEJXawxr8_nYhdHMyo130_assertion description "[Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94567.RAk_tVlLMbTug95cF3tt8muzLd_eEJXawxr8_nYhdHMyo130_provenance.
NP94574.RAg6DhRL2bepqB6QUtp-ixT8ujQuSBPIjmNTVKrdz5Thc130_assertion description "[Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94574.RAg6DhRL2bepqB6QUtp-ixT8ujQuSBPIjmNTVKrdz5Thc130_provenance.
NP94577.RAlqsL7Ismju5bvPmt7BcFotzmvEoz8DK2caUeCM9f1Zs130_assertion description "[Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94577.RAlqsL7Ismju5bvPmt7BcFotzmvEoz8DK2caUeCM9f1Zs130_provenance.
NP94580.RAlV7J59tlC_-JXhg3ZQ-5fipSYjod8u8MNjtzzxvb15w130_assertion description "[Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94580.RAlV7J59tlC_-JXhg3ZQ-5fipSYjod8u8MNjtzzxvb15w130_provenance.
NP94582.RAmGxFW5gOkP7AM3QgkoSHMHn2zLc6ry9137hx1RAVB_A130_assertion description "[Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94582.RAmGxFW5gOkP7AM3QgkoSHMHn2zLc6ry9137hx1RAVB_A130_provenance.
NP94586.RAubzXO9aW4s9-2EoKr-ZF38XRJPljhO1sQdUQI7Exors130_assertion description "[Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94586.RAubzXO9aW4s9-2EoKr-ZF38XRJPljhO1sQdUQI7Exors130_provenance.
NP94608.RAlc-IUDfdR1Jbfe8ecsF73WN7uF7oXKTTL7qkliDBffA130_assertion description "[Susceptibility loci for intracranial aneurysm in European and Japanese populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94608.RAlc-IUDfdR1Jbfe8ecsF73WN7uF7oXKTTL7qkliDBffA130_provenance.
NP94611.RAtLK0aHToUMytiZ7_ePn8kfjeVMJIGqB7LIX5oho0-6A130_assertion description "[Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94611.RAtLK0aHToUMytiZ7_ePn8kfjeVMJIGqB7LIX5oho0-6A130_provenance.
NP94619.RAlTgBPI7LXm-4mlH0NAKkbIkEs6PsmWo0niCOqyg1iqo130_assertion description "[Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94619.RAlTgBPI7LXm-4mlH0NAKkbIkEs6PsmWo0niCOqyg1iqo130_provenance.
NP94623.RAvudl7mJk8IoTqZOGv_DImmIotm01IPipR3rfAjU9ixg130_assertion description "[Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94623.RAvudl7mJk8IoTqZOGv_DImmIotm01IPipR3rfAjU9ixg130_provenance.
NP94629.RApet5x08olldpUWNixdNmMhVOC-uLMQP49HF5lZzmxro130_assertion description "[Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94629.RApet5x08olldpUWNixdNmMhVOC-uLMQP49HF5lZzmxro130_provenance.
NP94632.RAtplNWj0FhHUlyWHuZbcF5h-7r2eMO0TElgDjys-NOtA130_assertion description "[Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94632.RAtplNWj0FhHUlyWHuZbcF5h-7r2eMO0TElgDjys-NOtA130_provenance.
NP94634.RAp1TcEvAydWQTKfpeUPYJnwIZe6Z6JQbvSkHVh3-sbtE130_assertion description "[Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94634.RAp1TcEvAydWQTKfpeUPYJnwIZe6Z6JQbvSkHVh3-sbtE130_provenance.
NP94636.RAsMwL02zkZr5H-pmdwHEeEhLWkwdW_mgTsge8XXcyXu8130_assertion description "[Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94636.RAsMwL02zkZr5H-pmdwHEeEhLWkwdW_mgTsge8XXcyXu8130_provenance.
NP94639.RAir-k5Shm0V6KB-hcx0jOp-RZtyQBQUmL0CcUMvLHmbo130_assertion description "[Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94639.RAir-k5Shm0V6KB-hcx0jOp-RZtyQBQUmL0CcUMvLHmbo130_provenance.
NP94640.RAls0PCe1QhBkMg8-IvX2zUhpIm8N9C3y47p2ArtpuxAQ130_assertion description "[Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94640.RAls0PCe1QhBkMg8-IvX2zUhpIm8N9C3y47p2ArtpuxAQ130_provenance.
NP94644.RAvuYd8pINsguxMaTiv7lVIzpz8LkqJrNGd2RZZc5zXVM130_assertion description "[Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94644.RAvuYd8pINsguxMaTiv7lVIzpz8LkqJrNGd2RZZc5zXVM130_provenance.
NP94645.RAujd1un712dzV2sAGHwtEPD4A8g26QKag2TgF3DkbjxA130_assertion description "[Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94645.RAujd1un712dzV2sAGHwtEPD4A8g26QKag2TgF3DkbjxA130_provenance.
NP94650.RAtfFby5lQaBzs32Mf3QE7NE6AAezM7LGKOBqErJ0zG64130_assertion description "[Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94650.RAtfFby5lQaBzs32Mf3QE7NE6AAezM7LGKOBqErJ0zG64130_provenance.
NP94666.RArVSEwR1xO1L95uwRnOeB7cggkIARXyr651r6LlDArr0130_assertion description "[The polymorphic codon 129 of PRNP was the main genetic risk factor for vCJD; however, additional candidate loci have been identified, which justifies functional analyses of these biological pathways in prion disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94666.RArVSEwR1xO1L95uwRnOeB7cggkIARXyr651r6LlDArr0130_provenance.
NP94668.RAj5DNqEVtTZ9i1OXtj2qtA_YR_kxyA-3qqZo5TmFyscE130_assertion description "[Genomewide association study of an AIDS-nonprogression cohort emphasizes the role played by HLA genes (ANRS Genomewide Association Study 02).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94668.RAj5DNqEVtTZ9i1OXtj2qtA_YR_kxyA-3qqZo5TmFyscE130_provenance.
NP94670.RAtgKnHEXrB1-EvPqCzjGLS9doP-sj_AwjU-ibfM1BmzE130_assertion description "[Genomewide association study of an AIDS-nonprogression cohort emphasizes the role played by HLA genes (ANRS Genomewide Association Study 02).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94670.RAtgKnHEXrB1-EvPqCzjGLS9doP-sj_AwjU-ibfM1BmzE130_provenance.
NP94671.RAqHi4nfQg3q_Vut9dhpWCnYlCoF3bdRQUs_mniLklwdE130_assertion description "[Sequence variants at 22q13 are associated with prostate cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94671.RAqHi4nfQg3q_Vut9dhpWCnYlCoF3bdRQUs_mniLklwdE130_provenance.
NP94674.RAjEmo9V1bOqoyvfrWqlyhSGU0mcv0wBf455HjoWFkOaY130_assertion description "[Genome-wide association identifies multiple ulcerative colitis susceptibility loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94674.RAjEmo9V1bOqoyvfrWqlyhSGU0mcv0wBf455HjoWFkOaY130_provenance.
NP94675.RAnhefQkkcwQSZDCofRpO7lqr1hhNQvCmhNmj7R6LtpUQ130_assertion description "[Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94675.RAnhefQkkcwQSZDCofRpO7lqr1hhNQvCmhNmj7R6LtpUQ130_provenance.

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