Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP47632.RAsEss2Wg2OK-U7aOXXvvcnGxzzHbCLhjgdofTqcBRxfE130_assertion description "[In addition, a pooled analysis of existing published and unpublished data in 1305 cases of SLE genotyped for the CARD15 risk alleles suggests that only the CARD15(908R) IBD risk allele may have a strong effect on risk of SLE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47632.RAsEss2Wg2OK-U7aOXXvvcnGxzzHbCLhjgdofTqcBRxfE130_provenance.
- NP47634.RAtK7DhjmgJCAY4sFN6Ev1oeHYt77LKbCupUXy_Lpn-Bk130_assertion description "[VLBW infants with repeated episodes of sepsis had higher frequencies of the NOD2-3020insC and IL6-174G allele.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47634.RAtK7DhjmgJCAY4sFN6Ev1oeHYt77LKbCupUXy_Lpn-Bk130_provenance.
- NP47636.RAiHf7jQN9lEBNMF-BGcaPBfshT6dUQLEiDz0F8HM7wjg130_assertion description "[The increased sepsis rate of homozygous IL6-174G carriers was especially related to an increase in Gram-positive infections, and was not observed in VLBW infants who received prophylaxis with teicoplanin (frequency of Gram-positive sepsis in homozygous IL6-174G carriers without prophylaxis 16.5% versus 2.4% in homozygous IL6-174G carriers with prophylaxis; p = 0.033).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47636.RAiHf7jQN9lEBNMF-BGcaPBfshT6dUQLEiDz0F8HM7wjg130_provenance.
- NP47643.RAnd_B8nS7zk2yanDsJ0s57Gn9y39SbOKOvf56vtP2XX4130_assertion description "[Association between calpain-10 gene polymorphism and risk of type 2 diabetes mellitus: a meta analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47643.RAnd_B8nS7zk2yanDsJ0s57Gn9y39SbOKOvf56vtP2XX4130_provenance.
- NP47649.RAttS-ZOlvcQXdCR0t5kphdZnv2wY_mXp0XahveujYZmc130_assertion description "[These results support a role of Calpain 10 gene in PCOS susceptibility in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47649.RAttS-ZOlvcQXdCR0t5kphdZnv2wY_mXp0XahveujYZmc130_provenance.
- NP47662.RAqVJRtHNuaT6ZrAwcE43vVIfYFeWR6GJoRz8giDejC-4130_assertion description "[Calcitonin gene polymorphism CALCA-624 (T/C) and ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47662.RAqVJRtHNuaT6ZrAwcE43vVIfYFeWR6GJoRz8giDejC-4130_provenance.
- NP47669.RAn8gAiuEn_xKs7JPZ3pZc2AMOZ8biLXDlFI00UgX4FOA130_assertion description "[Common polymorphisms in the CACNA1H gene associated with childhood absence epilepsy in Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47669.RAn8gAiuEn_xKs7JPZ3pZc2AMOZ8biLXDlFI00UgX4FOA130_provenance.
- NP47670.RAnIacUcOGR0_8nbCybzwR7pHVQjZbFZNzEfvYNJPceCA130_assertion description "[Molecular analysis of Spinocerebellar ataxias in Koreans: frequencies and reference ranges of SCA1, SCA2, SCA3, SCA6, and SCA7.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47670.RAnIacUcOGR0_8nbCybzwR7pHVQjZbFZNzEfvYNJPceCA130_provenance.
- NP47671.RAkccpvokO-9koCiQ8W_PD3Ynyk5n212-qQMxhfm2Dozk130_assertion description "[We conclude that total number of CAG repeat-units in both alleles is a good parameter for assessment of age of onset in SCA6 including homozygous patients. In addition, clinical and neuro-otological examinations suggested that SCA6 is a disease with predominantly cerebellar dysfunction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47671.RAkccpvokO-9koCiQ8W_PD3Ynyk5n212-qQMxhfm2Dozk130_provenance.
- NP47673.RAtlet-pojUh63ejfnDml-lGH4q_kS2c8j6zV-TB_IiBc130_assertion description "[To evaluate the contribution of SCA alleles to idiopathic RLS we investigated the CAG repeat length at the SCA1, SCA2, SCA3, SCA6, SCA7, and SCA17 loci in 215 patients who fulfilled the clinical criteria of RLS and presented periodic leg movements in sleep (PLMS) in polysomnographic recording.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47673.RAtlet-pojUh63ejfnDml-lGH4q_kS2c8j6zV-TB_IiBc130_provenance.
- NP47680.RAiQrOkDCZMcoi6aybLSr4Gyh7JBhp-gsBgUyRhaIXQpg130_assertion description "[Complement component C7 deficiency in a Spanish family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47680.RAiQrOkDCZMcoi6aybLSr4Gyh7JBhp-gsBgUyRhaIXQpg130_provenance.
- NP47681.RAlv-v_unu-sknRA0tgBN_dDE4KrGSZSmiuwA22jCPsZI130_assertion description "[Five new polymorphisms in the complement C7 gene and their association with C7 deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47681.RAlv-v_unu-sknRA0tgBN_dDE4KrGSZSmiuwA22jCPsZI130_provenance.
- NP47688.RArwM8RyeYw5NjgUxGWLvxDZf-ZG9YO5sxhHX6QEUphYs130_assertion description "[These results suggest that the C3 and C5 pathways of the complement system play important roles in the pathogenesis of BA and that polymorphisms of these genes affect susceptibility to BA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47688.RArwM8RyeYw5NjgUxGWLvxDZf-ZG9YO5sxhHX6QEUphYs130_provenance.
- NP47691.RAnCXUCbtqhvbCQ9kw1xvmphxmXOZOJ5jO_LBO8LIVQdE130_assertion description "[A patient-only association study suggested that severity of childhood BA was associated with 1526G/A of the C3AR1 gene (P = 0.0057).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47691.RAnCXUCbtqhvbCQ9kw1xvmphxmXOZOJ5jO_LBO8LIVQdE130_provenance.
- NP47695.RAtA_Ww0LpcGCpsn1Wkxc04-TzUhvSaZJyrQiKhgJlUN4130_assertion description "[The link of C4B null allele to autism and to a family history of autoimmunity in Egyptian autistic children.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47695.RAtA_Ww0LpcGCpsn1Wkxc04-TzUhvSaZJyrQiKhgJlUN4130_provenance.
- NP47697.RAoDKC4h9FoEm1DzMk5LVuc26xB8a41EGgeuF2GZAqfdc130_assertion description "[Association between C3 complement types and bronchial asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47697.RAoDKC4h9FoEm1DzMk5LVuc26xB8a41EGgeuF2GZAqfdc130_provenance.
- NP47699.RApw3yL1AtNbto9gjApQSQ3rhmWehuSftEOfgW2eHjsNc130_assertion description "[Based on the results obtained, a genetic control was assumed for the development of the tuberculosis process in the lungs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47699.RApw3yL1AtNbto9gjApQSQ3rhmWehuSftEOfgW2eHjsNc130_provenance.
- NP47701.RAtba9TiOMbZ1JuNB4ffb7tBHyxLuiCMUvVcExY5Q2Jvo130_assertion description "[High-density SNP screening of the major histocompatibility complex in systemic lupus erythematosus demonstrates strong evidence for independent susceptibility regions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47701.RAtba9TiOMbZ1JuNB4ffb7tBHyxLuiCMUvVcExY5Q2Jvo130_provenance.
- NP47704.RAqu2mkK7xHvcIpsIA3fjnpDe6ZTIvfu-38EwXOaNAuOU130_assertion description "[A polymorphism in the complement component C1r is not associated with sporadic Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47704.RAqu2mkK7xHvcIpsIA3fjnpDe6ZTIvfu-38EwXOaNAuOU130_provenance.
- NP47705.RApxoBFu5VDnabMCvCtjzR1Htpe2i2f59SrhxzKEZX29M130_assertion description "[Our data suggest that the LBP-1c/CP2/LSF polymorphism may have a moderate protective effect against the risk of AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47705.RApxoBFu5VDnabMCvCtjzR1Htpe2i2f59SrhxzKEZX29M130_provenance.
- NP47707.RAr85U697sRLSv_IkSyiotQ4wVh-lvrgoPxeHSXl9V3aM130_assertion description "[ This study shows an association between a nonsynonymous change (H6D) in the MIC-1 gene and prostate cancer. This finding supports the hypothesis that genetic variation in the inflammatory process contributes to prostate cancer susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47707.RAr85U697sRLSv_IkSyiotQ4wVh-lvrgoPxeHSXl9V3aM130_provenance.
- NP47712.RAl6LCCHoEBQNAaZkWrDFbD8QWXaWBXrez7oyRkLZ-VIs130_assertion description "[Here, we carried out a systematic three-stage SNP scan of 16.4 Mb on chromosome 6p21 in as many as 947 independent cases of familial and sporadic sarcoidosis and found that a 15-kb segment of the gene butyrophilin-like 2 (BTNL2) was associated with the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47712.RAl6LCCHoEBQNAaZkWrDFbD8QWXaWBXrez7oyRkLZ-VIs130_provenance.
- NP47715.RAmDHLT1_O66RD3heFeND2AP56B_EHTvOPVGbaqovvhnw130_assertion description "[Analysis of BTNL2 genetic polymorphisms in British and Dutch patients with sarcoidosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47715.RAmDHLT1_O66RD3heFeND2AP56B_EHTvOPVGbaqovvhnw130_provenance.
- NP47717.RAjeKYriOzsr6I-s_G2xuTrkijG3yHyRghwlPM8Gf1Apk130_assertion description "[Analysis of multiple candidate genes in association with phenotypes of multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47717.RAjeKYriOzsr6I-s_G2xuTrkijG3yHyRghwlPM8Gf1Apk130_provenance.
- NP47720.RArLNrKmNehLxDe_KXvLdSnLW4ixn1RII4t7-D3IxXjIc130_assertion description "[Real time PCR assays to detect common mutations in the biotinidase gene and application of mutational analysis to newborn screening for biotinidase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47720.RArLNrKmNehLxDe_KXvLdSnLW4ixn1RII4t7-D3IxXjIc130_provenance.
- NP47725.RAqarU1h41YkCDlGORRZJusq8YJS0b1vJR0Wi3bvCEE7s130_assertion description "[Given the growing evidence now linking BRCA1, BRCA2, and the FA pathway, as well as the involvement of FA proteins (BRCA2/FANCD1 and PALB2/FANCN) in breast cancer susceptibility, we sought to evaluate the contribution of FANCJ gene alterations regarding breast cancer susceptibility among our cohort of 96 breast cancer individuals from high-risk non-BRCA1/2 French Canadian families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47725.RAqarU1h41YkCDlGORRZJusq8YJS0b1vJR0Wi3bvCEE7s130_provenance.
- NP47726.RAglVwmdIaoTm3h8t9r4LUkePt96sjz2wcJOdc3EdJvHE130_assertion description "[there was little evidence of breast cancer susceptibility with any of the SNPs studied, but larger studies would be needed to confirm subgroup effects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47726.RAglVwmdIaoTm3h8t9r4LUkePt96sjz2wcJOdc3EdJvHE130_provenance.
- NP47727.RArXcw_8L__dluEvHzCMVfMJ9DTL4DEUBxQNcKIXhQ5GY130_assertion description "[The Fanconi anemia family of genes and its correlation with breast cancer susceptibility and breast cancer features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47727.RArXcw_8L__dluEvHzCMVfMJ9DTL4DEUBxQNcKIXhQ5GY130_provenance.
- NP47730.RAmuksN06UI6mnIvN3ejJWr1GNF5ue-tfb7PnWgQZTaWw130_assertion description "[Screening for large genomic rearrangements of the BRIP1 and CHK1 genes in Finnish breast cancer families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47730.RAmuksN06UI6mnIvN3ejJWr1GNF5ue-tfb7PnWgQZTaWw130_provenance.
- NP47740.RAvSpbaeR1_4TdT1t4_5mGLpCBJMjkNnbS2E6bb6f4Rcg130_assertion description "[The LSP1 and 2q35 SNPs appear to interact multiplicatively on breast cancer risk for BRCA2 mutation carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47740.RAvSpbaeR1_4TdT1t4_5mGLpCBJMjkNnbS2E6bb6f4Rcg130_provenance.
- NP47744.RAqEFm46e9d-sNjO5ezFjUgnzalJgKP3QKjra_7NptFcI130_assertion description "[Our results suggest that variant genotypes of the Thr1915Met and Met784Val polymorphisms of the BRCA2 gene may be indicative factors in therapy of ductal breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47744.RAqEFm46e9d-sNjO5ezFjUgnzalJgKP3QKjra_7NptFcI130_provenance.
- NP47749.RAp17Zo5g5HgpRHQYj1vTQb2mukJ3lj7EMab66R8VRAKs130_assertion description "[Common genetic variation at the 9p22.2 locus was associated with decreased risk of ovarian cancer for carriers of a BRCA1 or BRCA2 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47749.RAp17Zo5g5HgpRHQYj1vTQb2mukJ3lj7EMab66R8VRAKs130_provenance.
- NP47754.RAqusCNbAolsY0XYY008j9p-WYRd4blQNeDPZzrHpMhDA130_assertion description "[BRCA1 and BRCA2 mutations account for an important fraction of hereditary breast and ovarian cancer cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47754.RAqusCNbAolsY0XYY008j9p-WYRd4blQNeDPZzrHpMhDA130_provenance.
- NP47758.RAs7rFQPjS0mhZFlUw2hrph2ZAfCoCb5XduB9rbz2POSc130_assertion description "[The possible modifying effect on MBC risk in subjects carrying BRCA1/2 germ-line mutations of an occupation characterised by exposure to chemicals such as polycyclic aromatic hydrocarbons (PAH) that are capable of inducing DNA damage, may provide clues to the role of environmental exposures in modifying BC risk in mutation carriers in both genders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47758.RAs7rFQPjS0mhZFlUw2hrph2ZAfCoCb5XduB9rbz2POSc130_provenance.
- NP47762.RAvWza76yPOUrwWQA5l5JI_JTThl0fsi2rzj-lAyTnxfs130_assertion description "[Evaluation of BRCA2 in the genetic susceptibility of familial esophageal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47762.RAvWza76yPOUrwWQA5l5JI_JTThl0fsi2rzj-lAyTnxfs130_provenance.
- NP47764.RAk7p0VkcCfp9aqQeLa-vqWgLe-B0u79Ce6ZxyvrENtxA130_assertion description "[Germ-line variants in the NBS1 gene may play a role in the lung carcinogenesis in cigarette smokers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47764.RAk7p0VkcCfp9aqQeLa-vqWgLe-B0u79Ce6ZxyvrENtxA130_provenance.
- NP47765.RAi7Lqc1pmvlkRPBgDiURovXr47MZjnfVfL-LTZwPQ5_o130_assertion description "[Variants in the GH-IGF axis confer susceptibility to lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47765.RAi7Lqc1pmvlkRPBgDiURovXr47MZjnfVfL-LTZwPQ5_o130_provenance.
- NP47771.RAjyUCHzobsDwF5D2twZm3rYYjNErU7FwvfK6aq7X8YEU130_assertion description "[Prophylactic mastectomy in BRCA1 and BRCA2 mutation carriers: very low risk for subsequent breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47771.RAjyUCHzobsDwF5D2twZm3rYYjNErU7FwvfK6aq7X8YEU130_provenance.
- NP47774.RAvvtbVdO3yuance5uMNgvIiOMDCcnOQj_paV0lZ7UQ58130_assertion description "[A study of Chinese women recently suggested that the minor allele of rs11655505 in the BRCA1 promoter (c.-2265C-->T) increases promoter activity and has a protective effect on breast cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47774.RAvvtbVdO3yuance5uMNgvIiOMDCcnOQj_paV0lZ7UQ58130_provenance.
- NP47792.RAuF1GaMeG2ZjRbX7igA_7Ifx-uuy54XD8GaKG7a7dp10130_assertion description "[Mutation screening of the phosducin gene PDC in patients with retinitis pigmentosa and allied diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47792.RAuF1GaMeG2ZjRbX7igA_7Ifx-uuy54XD8GaKG7a7dp10130_provenance.
- NP47795.RAtkTVqnmC9mo6wX0a1dTqG_yojH_cXaffuebwhrKA3RE130_assertion description "[Frequency of BRCA1 and BRCA2 mutations in unselected Ashkenazi Jewish patients with colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47795.RAtkTVqnmC9mo6wX0a1dTqG_yojH_cXaffuebwhrKA3RE130_provenance.
- NP47798.RAi7el_RloErk5ktH-eE5hN8oarGqMvKeZQ9wL1v-Zi5k130_assertion description "[The frequency of the predominant Jewish mutations in BRCA1 and BRCA2 in unselected Ashkenazi colorectal cancer patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47798.RAi7el_RloErk5ktH-eE5hN8oarGqMvKeZQ9wL1v-Zi5k130_provenance.
- NP47808.RAjlETXX53e3KSDgkUATy-dcLhe-6d8nChLGQcwOwB2q4130_assertion description "[Study of the BMPR2 gene in patients with pulmonary arterial hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47808.RAjlETXX53e3KSDgkUATy-dcLhe-6d8nChLGQcwOwB2q4130_provenance.
- NP47812.RAnuu-ZtSI7OL9Th7wOYO0MA-_mfCNpe8_Q8oeKVnD55k130_assertion description "[Mutation screening in juvenile polyposis syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47812.RAnuu-ZtSI7OL9Th7wOYO0MA-_mfCNpe8_Q8oeKVnD55k130_provenance.
- NP47821.RAmkMGXGH-Yt6Leo0QL5TIMB6McWXOtlFDcbyvZOqlrKw130_assertion description "[Bloom's syndrome (BS), a human recessive disorder associated with an increased risk of malignancy, arises through mutations in both alleles of the BLM gene, which was recently identified as a member of the RecQ helicase family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47821.RAmkMGXGH-Yt6Leo0QL5TIMB6McWXOtlFDcbyvZOqlrKw130_provenance.
- NP47823.RAgG3DSdx8fMYczzo-1qfX4yHBTu0FSjlqKUkmKteHxlM130_assertion description "[ Based on our results, we conclude that the HindIII polymorphism of the osteocalcin gene is a suitable genetic marker of prostate cancer which can be used in the prediction of the outcome of patients who receive hormone therapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47823.RAgG3DSdx8fMYczzo-1qfX4yHBTu0FSjlqKUkmKteHxlM130_provenance.
- NP47826.RArhfuGZzBbrj1v6Lmq3xPsZMCkrbMB5Igi_9zEvb0vpE130_assertion description "[Bf polymorphisms in systemic lupus erythematosus patients of Spanish descent.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47826.RArhfuGZzBbrj1v6Lmq3xPsZMCkrbMB5Igi_9zEvb0vpE130_provenance.
- NP47827.RAhGBFiOnRPyhDdkRls2NLvqEmKCKgU2b0PWI2AZNuIZ4130_assertion description "[High-density SNP screening of the major histocompatibility complex in systemic lupus erythematosus demonstrates strong evidence for independent susceptibility regions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47827.RAhGBFiOnRPyhDdkRls2NLvqEmKCKgU2b0PWI2AZNuIZ4130_provenance.
- NP47830.RAnnAF3ZDiOZqxndef4ASpYlMfeYORwIn3UIBvvz4ru7U130_assertion description "[ These results support the hypothesis that the African-American population is an older population compared with the other samples and the two bradykinin receptors may play a role in blood pressure regulation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47830.RAnnAF3ZDiOZqxndef4ASpYlMfeYORwIn3UIBvvz4ru7U130_provenance.
- NP47832.RAscbbYmIhT2TAk2XBWzW6VmTwdzfyiMblSUZgqDlmh2c130_assertion description "[ B2R genotype can explain part of the BRS variation that is unaccounted for by simple anthropometric variables and common risk factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47832.RAscbbYmIhT2TAk2XBWzW6VmTwdzfyiMblSUZgqDlmh2c130_provenance.
- NP47839.RArIARQrwTGvulYB5CxPO90u6k_GVsABSd3Nlo8EkX3C4130_assertion description "[Thus, the B2R exon 1 polymorphism may represent a susceptibility marker for nephropathy progression in diabetic patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47839.RArIARQrwTGvulYB5CxPO90u6k_GVsABSd3Nlo8EkX3C4130_provenance.
- NP47840.RArcyxQ8z3wxCQfjGfwiAHYlJs_vSK8uuG_gETe-ptDEM130_assertion description "[The coronary risk attributable to systolic hypertension (SBP>/=160 mmHg) was significantly higher only in B(1)R-699GG homozygotes (HR 2.14 1.42-3.22; P<0.0001) and B(2)R(+9,+9) individuals (HR 3.51 1.69-7.28; P=0.001) but not in B(1)R-699C allele carriers (HR 0.82 0.28-2.42; P=0.76) or in B(2)R(-9,-9) homozygotes (HR 1.25 0.51-3.04; P=0.63).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47840.RArcyxQ8z3wxCQfjGfwiAHYlJs_vSK8uuG_gETe-ptDEM130_provenance.
- NP47847.RAufALqljmiHFVnXEh0_92ahDsc9Qn4NGzmZiUrzN7nGU130_assertion description "[The coronary risk attributable to systolic hypertension (SBP>/=160 mmHg) was significantly higher only in B(1)R-699GG homozygotes (HR 2.14 1.42-3.22; P<0.0001) and B(2)R(+9,+9) individuals (HR 3.51 1.69-7.28; P=0.001) but not in B(1)R-699C allele carriers (HR 0.82 0.28-2.42; P=0.76) or in B(2)R(-9,-9) homozygotes (HR 1.25 0.51-3.04; P=0.63).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47847.RAufALqljmiHFVnXEh0_92ahDsc9Qn4NGzmZiUrzN7nGU130_provenance.
- NP47855.RAn4NwVRoHKUup-7QM4jt9D4V-xSOEDtPrukkiPKewm0o130_assertion description "[Variants of B cell lymphoma 6 (BCL6) and marked atopy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47855.RAn4NwVRoHKUup-7QM4jt9D4V-xSOEDtPrukkiPKewm0o130_provenance.
- NP47856.RAq26o8YWoh9cGYfMteBU6QHSIbkjDB7OijTRgEhSNqW0130_assertion description "[No significant differences in the frequency of gene sequence variations were found between MS patients and controls. The apoptosis genes studied here therefore appear less likely to be important effector genes in MS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47856.RAq26o8YWoh9cGYfMteBU6QHSIbkjDB7OijTRgEhSNqW0130_provenance.
- NP47858.RAvOrcKQVlAZNkGupB9x6n7wEW7wUNP4Di-rUAH9ddTVQ130_assertion description "[ Bcl-2 gene polymorphism is associated with SLE and may be directly involved in the process of SLE or in linkage disequilibrium with some susceptibility loci nearby. Synergistic effect may exist between IL-10 and bcl-2 genotypes in determining susceptibility to SLE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47858.RAvOrcKQVlAZNkGupB9x6n7wEW7wUNP4Di-rUAH9ddTVQ130_provenance.
- NP47863.RAtJpIR3dpvd1mwlo1SmgkezvOLujcrQindE-fVIUwjtU130_assertion description "[Association analysis with microsatellite and SNP markers does not support the involvement of BCL-2 in systemic lupus erythematosus in Mexican and Swedish patients and their families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47863.RAtJpIR3dpvd1mwlo1SmgkezvOLujcrQindE-fVIUwjtU130_provenance.
- NP47865.RAhPYFLX5EGi5WPRBvxD4vwh9idF1LHOCMBw_1Nk5g5y0130_assertion description "[ Bcl-2 gene polymorphism is associated with SLE and may be directly involved in the process of SLE or in linkage disequilibrium with some susceptibility loci nearby. Synergistic effect may exist between IL-10 and bcl-2 genotypes in determining susceptibility to SLE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47865.RAhPYFLX5EGi5WPRBvxD4vwh9idF1LHOCMBw_1Nk5g5y0130_provenance.
- NP47871.RApc4x8mzpoNMwz_C3nGqWv-ymh78SJ8ghdBIrbHpMqtA130_assertion description "[These findings suggested that a limited number of mutations might underlie MSUD in the AJ population, potentially facilitating prenatal diagnosis and carrier detection of MSUD in this group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47871.RApc4x8mzpoNMwz_C3nGqWv-ymh78SJ8ghdBIrbHpMqtA130_provenance.
- NP47875.RArKxrhBAjpp16Mm2mbbbUlvQ0pSWl4AdQNnWsoLvQkzQ130_assertion description "[Alzheimer's disease (AD) is characterized by a significant reduction in AcetylCholinesterase and an increase in ButyrylCholinesterase (BuChE) activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47875.RArKxrhBAjpp16Mm2mbbbUlvQ0pSWl4AdQNnWsoLvQkzQ130_provenance.
- NP47877.RAqmkaEIcENnevf2Qi-4ZF_3T6oMSXTZa3QGkiUt0IjHI130_assertion description "[In a case-control study in 231 AD patients and 221 healthy controls, we examined whether the combined effects between 14-3-3 zeta (rs964917 and rs983583) and BCHE (K variant) polymorphisms might be responsible for susceptibility to AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47877.RAqmkaEIcENnevf2Qi-4ZF_3T6oMSXTZa3QGkiUt0IjHI130_provenance.
- NP47878.RAuIN4AaNTc_nUWDAqYWk5vb6b0-VG9qUZC0zQ0qWWx40130_assertion description "[Synergistic effect of apolipoprotein E epsilon4 and butyrylcholinesterase K-variant on progression from mild cognitive impairment to Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47878.RAuIN4AaNTc_nUWDAqYWk5vb6b0-VG9qUZC0zQ0qWWx40130_provenance.
- NP47886.RApywUoM-cDkFwUV4v_gXR_qMgGmEXQSoSkZu7AfBIi14130_assertion description "[There is evidence to suggest an involvement of the K variant of the butyrylcholinesterase gene (BCHE) in dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47886.RApywUoM-cDkFwUV4v_gXR_qMgGmEXQSoSkZu7AfBIi14130_provenance.
- NP47892.RAtZaaAsPRBMkhJKEqXS4f6_3B8ZOXiv2Xl_PGoVH2SmE130_assertion description "[ The data suggest that genetic determinants of response to infliximab therapy exist in the HLA complex.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47892.RAtZaaAsPRBMkhJKEqXS4f6_3B8ZOXiv2Xl_PGoVH2SmE130_provenance.
- NP47893.RAg9Ngk79R2cs1inczURWTG8AQCJwWSEbNaIIXCWn6row130_assertion description "[ The above-mentioned pattern, most likely formed by recombination of the telomeric fragment of the MHC 7.1 ancestral haplotype, seems to be the most important genetic determinant of susceptibility to the extensive form of UC in our population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47893.RAg9Ngk79R2cs1inczURWTG8AQCJwWSEbNaIIXCWn6row130_provenance.
- NP47899.RArfovDBygQiFHRBOQ2h2iMJE99dkTixXbgFP2Sn3KWGc130_assertion description "[These results suggest that the contribution of the BARD1 germline variants to breast cancer predisposition is very limited, and that neither Cys557Ser nor Val507Met have an effect on familial breast cancer susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47899.RArfovDBygQiFHRBOQ2h2iMJE99dkTixXbgFP2Sn3KWGc130_provenance.
- NP47910.RAiDDIVl3XbpI2BRszFgT-pVEypJn136iJvzUVHRVa2AA130_assertion description "[The multifactorial genetic dysfunction in AD includes mutational loci (APP, PS1, PS2) and diverse susceptibility loci (APOE, A2M, AACT, LRP1, IL1A, TNF, ACE, BACE, BCHE, CST3, MTHFR, GSK3B, NOS3) distributed across the human genome, probably converging in common pathogenic mechanisms that lead to premature neuronal death.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47910.RAiDDIVl3XbpI2BRszFgT-pVEypJn136iJvzUVHRVa2AA130_provenance.
- NP47914.RAvX9ezA0PgCtjdL6_oTAh9HhFKEmn27PJRy4G_af7Nog130_assertion description "[BACE1 polymorphisms do not influence platelet membrane beta-secretase activity or genetic susceptibility for Alzheimer's disease in the Northern Irish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47914.RAvX9ezA0PgCtjdL6_oTAh9HhFKEmn27PJRy4G_af7Nog130_provenance.
- NP47924.RAoIMIV7qHI788J-GCWgi-B9bMhIxGyrdUhL53v9KY7Rs130_assertion description "[Spinocerebellar ataxias: microsatellite and allele frequency in unaffected and affected individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47924.RAoIMIV7qHI788J-GCWgi-B9bMhIxGyrdUhL53v9KY7Rs130_provenance.
- NP47926.RAsBHtGJYWdwSkf-Z85_MmuX6KrDVY4LqzFkPxq6JaSGc130_assertion description "[A de novo mutation in the coding sequence for neurophysin-II (Pro24-->Leu) is associated with onset and transmission of autosomal dominant neurohypophyseal diabetes insipidus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47926.RAsBHtGJYWdwSkf-Z85_MmuX6KrDVY4LqzFkPxq6JaSGc130_provenance.
- NP47927.RAsAqgMLbbZbV5Xv5dXuEb-KMvzJJTXUquWvFBM_3lMVY130_assertion description "[A partial defect in AVP secretion occurs early in the course of FNDI and may not be detected by a water deprivation test (WDT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47927.RAsAqgMLbbZbV5Xv5dXuEb-KMvzJJTXUquWvFBM_3lMVY130_provenance.
- NP47934.RArNQD0KT-3C1w-T9gbez-DkNQdvpwDgsMhE6Pgiq2Fzg130_assertion description "[Molecular analysis of Spinocerebellar ataxias in Koreans: frequencies and reference ranges of SCA1, SCA2, SCA3, SCA6, and SCA7.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47934.RArNQD0KT-3C1w-T9gbez-DkNQdvpwDgsMhE6Pgiq2Fzg130_provenance.
- NP47936.RAr9iJ88_pWNwthDcrGVrLQ0mpW6HZdYlQ2qCZG_GegSs130_assertion description "[Molecular analysis of CAG repeats at five different spinocerebellar ataxia loci: correlation and alternative explanations for disease pathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47936.RAr9iJ88_pWNwthDcrGVrLQ0mpW6HZdYlQ2qCZG_GegSs130_provenance.
- NP47937.RAu9OJlu7IOH-b0VpEOOwIwsdwQdV_WiZmL2Dq8wfCnWA130_assertion description "[To evaluate the contribution of SCA alleles to idiopathic RLS we investigated the CAG repeat length at the SCA1, SCA2, SCA3, SCA6, SCA7, and SCA17 loci in 215 patients who fulfilled the clinical criteria of RLS and presented periodic leg movements in sleep (PLMS) in polysomnographic recording.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47937.RAu9OJlu7IOH-b0VpEOOwIwsdwQdV_WiZmL2Dq8wfCnWA130_provenance.
- NP47942.RAteEShj4e2B0tciZhc_e7m_rWlTVEcJhDkjCvzp9AbEQ130_assertion description "[In this study, we conducted genetic analysis of SCA2, 3, 17 in an ethnic Chinese cohort with early onset and familial Parkinson's disease (PD) and healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47942.RAteEShj4e2B0tciZhc_e7m_rWlTVEcJhDkjCvzp9AbEQ130_provenance.
- NP47954.RAj0u9984eaq-sPk9TnIt09M62EaKBRUXSNEppTWUmR0c130_assertion description "[Genetic analysis of Alzheimer's disease in the Uppsala Longitudinal Study of Adult Men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47954.RAj0u9984eaq-sPk9TnIt09M62EaKBRUXSNEppTWUmR0c130_provenance.
- NP47958.RAvSto3rVTwAkEXJXY4RauCDMXi3BDyM9c6Mm7ycN8KBQ130_assertion description "[Autosomal dominant cerebellar ataxias are a clinical and genetically heterogeneous group of progressive neurodegenerative diseases, at present associated with 22 loci (spinocerebellar ataxia SCA 1-SCA8, SCA10-SCA19, SCA21, SCA22, fibroblast growth factor 14 FGF14-SCA, and dentatorubral-pallidoluysian atrophy DRPLA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47958.RAvSto3rVTwAkEXJXY4RauCDMXi3BDyM9c6Mm7ycN8KBQ130_provenance.
- NP47960.RAs7BN3A7JosKNkRIdRfUJOAVJEbWM5cRZ9snoB7taI6g130_assertion description "[Autosomal dominant cerebellar ataxias are a clinical and genetically heterogeneous group of progressive neurodegenerative diseases, at present associated with 22 loci (spinocerebellar ataxia SCA 1-SCA8, SCA10-SCA19, SCA21, SCA22, fibroblast growth factor 14 FGF14-SCA, and dentatorubral-pallidoluysian atrophy DRPLA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47960.RAs7BN3A7JosKNkRIdRfUJOAVJEbWM5cRZ9snoB7taI6g130_provenance.
- NP47970.RAnKthig-X85l5vaXSFS-7Rx5SVE23krgRt6EBSoAcRUQ130_assertion description "[Here we have evaluated 62 WND cases (58 probands) from the Chinese Han population to expand our knowledge of ATP7B mutations and to more completely characterize WND in China.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47970.RAnKthig-X85l5vaXSFS-7Rx5SVE23krgRt6EBSoAcRUQ130_provenance.
- NP47974.RAnT7A4GbWjFdlZr3xjpkSI3GuS2MN6KQcn9NM-vR-f6c130_assertion description "[Neurological manifestations and ATP7B mutations in Wilson's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47974.RAnT7A4GbWjFdlZr3xjpkSI3GuS2MN6KQcn9NM-vR-f6c130_provenance.
- NP47977.RAkdAMI2nCwP4oxsgGxrCelLXzwsfEOYXUEwfogr45bLo130_assertion description "[We have identified 28 different mutations in the ATP7B gene, including six novel variations, in 120 unrelated Korean patients with WND.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47977.RAkdAMI2nCwP4oxsgGxrCelLXzwsfEOYXUEwfogr45bLo130_provenance.
- NP47980.RAoYIQNcyIV_dUvGrL3owio-GtnUy87Ldng8H7T83DKzA130_assertion description "[ATP8B1 mutations in British cases with intrahepatic cholestasis of pregnancy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47980.RAoYIQNcyIV_dUvGrL3owio-GtnUy87Ldng8H7T83DKzA130_provenance.
- NP47983.RAvEak_G0nXJ_EUdc3Ubjj9YVg2xutCaPHmkWLBSEqeXo130_assertion description "[The association between blood lead and blood pressure was stronger among persons who were homozygous for the variant allele. Genotype was also associated with hypertension (adjusted odds]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47983.RAvEak_G0nXJ_EUdc3Ubjj9YVg2xutCaPHmkWLBSEqeXo130_provenance.
- NP47984.RAhHn-NK9vRITfa94-TPOfFNkyxMkXcqP4A08xkFpFfIY130_assertion description "[The rs4961 polymorphism of the ADD1 gene is associated with essential hypertension, but the rs28933400 locus in the ATP1A2 gene may have no association with essential hypertension in the studied population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47984.RAhHn-NK9vRITfa94-TPOfFNkyxMkXcqP4A08xkFpFfIY130_provenance.
- NP47996.RAhxEPC1_CF-aJtT_zTdpCOd0j_uwiT7fr-1nYA-DYWPc130_assertion description "[Our results indicate that genetic polymorphisms affecting knee OA vary between populations (Japanese versus Caucasian) and sexes and indicate a role for ASPN, COMP, FRZB, and COL2A1 in Caucasians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47996.RAhxEPC1_CF-aJtT_zTdpCOd0j_uwiT7fr-1nYA-DYWPc130_provenance.
- NP47997.RAjYS_KpAMKntGwYSlwDCS8ed0WRQO02iLuFjF9oHJee8130_assertion description "[An association between osteoarthritis (OA) and functional polymorphisms in the aspartic acid (d) repeat of the asporin (ASPN) gene was reported in Japanese and Han Chinese populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47997.RAjYS_KpAMKntGwYSlwDCS8ed0WRQO02iLuFjF9oHJee8130_provenance.
- NP47998.RAiCnvFWxWrXh9LVJzpGaxFP-A0uneDSUmZLXV0EEZmTI130_assertion description "[Lack of replication is common and could be due to differences in study design, phenotype, populations examined or the occurrence of false positives in the initial study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47998.RAiCnvFWxWrXh9LVJzpGaxFP-A0uneDSUmZLXV0EEZmTI130_provenance.
- NP47999.RAsemdQ5_OwVeMNHRRV34CsnSVQANXxTxQSVUPFjVRO8c130_assertion description "[The current case-control analyses detected nominal associations between polyglutamine length variations in ASCL1 and PD (P=0.018), but supported neither the previously observed weak association between PHOX2B and general schizophrenia, nor other gene-disease correlations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47999.RAsemdQ5_OwVeMNHRRV34CsnSVQANXxTxQSVUPFjVRO8c130_provenance.
- NP48000.RAorp21lnYKwxpd6ZC0Qv8SMhrujnQ3TREsRcInkgrwG8130_assertion description "[To determine whether genetic variation in the coding region of the MASH1 gene plays a role in the etiology of PD Caucasian patients, we analyzed the whole coding region of the MASH1 gene in PD patients from North America.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48000.RAorp21lnYKwxpd6ZC0Qv8SMhrujnQ3TREsRcInkgrwG8130_provenance.
- NP48001.RAr10qhthA3EN9daGGcxHEMqOUYnUSH583Rf5GVCwbObM130_assertion description "[In this multicentre study, we examined the prevalence of two mutations in the arylsulfatase A (ARSA) gene, i.e., c.459+1G>A and p.P426L, in 384 unrelated European patients presenting with different types of metachromatic leukodystrophy (MLD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48001.RAr10qhthA3EN9daGGcxHEMqOUYnUSH583Rf5GVCwbObM130_provenance.
- NP48002.RAmVIhCF6g8h9tljMoTt4cCIjZcHupMZ90fj4uQBKr0dk130_assertion description "[Two novel mutations in the arylsulfatase A gene associated with juvenile (R390Q) and adult onset (H397Y) metachromatic leukodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48002.RAmVIhCF6g8h9tljMoTt4cCIjZcHupMZ90fj4uQBKr0dk130_provenance.
- NP48004.RAgTggsyv5xDNcjjDPKMS4AmjFojCaEivfKsubESpXGrk130_assertion description "[This study investigated the possible effect of the pseudodeficient N-glycosylation polymorphism of the arylsulfatase A (ASA) gene on alcohol dependence among Koreans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48004.RAgTggsyv5xDNcjjDPKMS4AmjFojCaEivfKsubESpXGrk130_provenance.
- NP48009.RAphaVFhzoa2bh1MYKR3r0luWoTXcR68_PmXelxd0V_3c130_assertion description "[Androgen receptor status predicts response to chemotherapy, not risk of breast cancer in Indian women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48009.RAphaVFhzoa2bh1MYKR3r0luWoTXcR68_PmXelxd0V_3c130_provenance.
- NP48010.RAiX000cXgjXfFFuEeFRSswfjOuG0wplJsvnvhPiRCs9c130_assertion description "[Association between androgen receptor gene CAG repeat polymorphism and breast cancer risk: a meta-analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48010.RAiX000cXgjXfFFuEeFRSswfjOuG0wplJsvnvhPiRCs9c130_provenance.
- NP48011.RAkuzo2Pi16lqjT2uoXWSPUAKXQlV80J3ctIEiGE4VCq0130_assertion description "[Interaction between estrogens and androgen receptor genes microsatellites, prostate-specific antigen and androgen receptor expressions in breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48011.RAkuzo2Pi16lqjT2uoXWSPUAKXQlV80J3ctIEiGE4VCq0130_provenance.
- NP48013.RAhxCno_pEab8d3LOtQGY9kC6Q2OrrQfOpLn3zs8BzidE130_assertion description "[We have demonstrated that several SNPs are associated with survival.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48013.RAhxCno_pEab8d3LOtQGY9kC6Q2OrrQfOpLn3zs8BzidE130_provenance.
- NP48014.RAvOXe7mDa4lxeWnL140VlwRimZfAy-IYyaZdpywAInkw130_assertion description "[ESR1, AR, body size, and breast cancer risk in Hispanic and non-Hispanic white women living in the Southwestern United States.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48014.RAvOXe7mDa4lxeWnL140VlwRimZfAy-IYyaZdpywAInkw130_provenance.
- NP48016.RAru_ZhQwZgBl-xpEkOqRx0pAa04VgwFIKSLQO4xdbBmE130_assertion description "[, an association for breast cancer risk between short (SS) alleles for the repeat variants of the ESR2 and AR genes was found in women of Greek descent.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48016.RAru_ZhQwZgBl-xpEkOqRx0pAa04VgwFIKSLQO4xdbBmE130_provenance.
- NP48017.RAif3IgLikExAjZnMrAqJTJ8AsNvZ3TNSfxfqnFUbi9Rw130_assertion description "[Androgen receptor gene CAG repeats, estrogen exposure status, and breast cancer susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48017.RAif3IgLikExAjZnMrAqJTJ8AsNvZ3TNSfxfqnFUbi9Rw130_provenance.
- NP48021.RAgfmxWqOMoUvWa4J6K3_JkIIlzzsRqc7aDwuKkZ7qlpM130_assertion description "[The data presented here provide further support for the association between schizophrenia and CAG repeat number polymorphism in SCA1 gene. The significant increase of the mean number of CAG repeats in schizophrenics was found also in the MJD1/SCA3 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48021.RAgfmxWqOMoUvWa4J6K3_JkIIlzzsRqc7aDwuKkZ7qlpM130_provenance.