Nanopublications

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

Showing items 53,001 to 53,100 of ±4,851,667 with 100 items per page.

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NP95938.RArzp9VYR6_37RPNtG5FAfT_4hDiZOLYnX9s90a-Vykhs130_assertion description "[Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP95938.RArzp9VYR6_37RPNtG5FAfT_4hDiZOLYnX9s90a-Vykhs130_provenance.
NP95942.RAkRqPws9J1_zAQ_kh7m3F2Un6qnSd4ePimI7XAoEv2n0130_assertion description "[Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP95942.RAkRqPws9J1_zAQ_kh7m3F2Un6qnSd4ePimI7XAoEv2n0130_provenance.
NP95943.RArOC4xcLxJHINuiZOggS8USYOaiT31yov_44GZnbzgRI130_assertion description "[A genome-wide association study of attempted suicide.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP95943.RArOC4xcLxJHINuiZOggS8USYOaiT31yov_44GZnbzgRI130_provenance.
NP95949.RAhQ1HlI30_rGFctJxn5f7vE9mWjcNUMM2hczN88UYOqM130_assertion description "[Common variation in GPC5 is associated with acquired nephrotic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP95949.RAhQ1HlI30_rGFctJxn5f7vE9mWjcNUMM2hczN88UYOqM130_provenance.
NP95952.RAtTHUqz4Ptkew_u5P7DeZKrhdQVVb4Run4ugKxsizYiY130_assertion description "[Meta-analysis of genome-wide association for migraine in six population-based European cohorts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP95952.RAtTHUqz4Ptkew_u5P7DeZKrhdQVVb4Run4ugKxsizYiY130_provenance.
NP95953.RAjj32RKGx9sQYtxJ38xVJYM7ER54obunrH_v-6fEpMAg130_assertion description "[Genetic risk for RA involves both population-specific loci as well as many shared genetic susceptibility loci in comparisons of Asian and European populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP95953.RAjj32RKGx9sQYtxJ38xVJYM7ER54obunrH_v-6fEpMAg130_provenance.
NP95956.RAofhwwzx-DLeDH10o_ixCqJoZcUEedK2E3GUXBYtISCg130_assertion description "[This GWAS identified two loci involved in sporadic DCM, one of them probably implicates BAG3. Our results show that rare mutations in BAG3 contribute to monogenic forms of the disease, while common variant(s) in the same gene are implicated in sporadic DCM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP95956.RAofhwwzx-DLeDH10o_ixCqJoZcUEedK2E3GUXBYtISCg130_provenance.
NP95957.RAuUztsP3O6MYIa0WkDF1KLxn-3-JNnK94O3R2U9FqpmE130_assertion description "[Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP95957.RAuUztsP3O6MYIa0WkDF1KLxn-3-JNnK94O3R2U9FqpmE130_provenance.
NP95959.RAjXE1XZjxIovU2h59H9utWD4Sco63zkhThm3SsC8_QcA130_assertion description "[Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP95959.RAjXE1XZjxIovU2h59H9utWD4Sco63zkhThm3SsC8_QcA130_provenance.
NP95961.RAkOgMQLaGy3uYOtwC1SoEC5OQ-mFaGlst6SDjntAXPTQ130_assertion description "[Our results underscore the importance of international efforts combining GWAS datasets to isolate genetic loci for complex diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP95961.RAkOgMQLaGy3uYOtwC1SoEC5OQ-mFaGlst6SDjntAXPTQ130_provenance.
NP95963.RArC2DVb3wLZ_Xyh8crOR4rUurPwltzA4UiPjKVt93zNs130_assertion description "[Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP95963.RArC2DVb3wLZ_Xyh8crOR4rUurPwltzA4UiPjKVt93zNs130_provenance.
NP95965.RAp0fQZZJOZ9JMuVtixmP_qfyfgNuWe6hvLpVTWohXCAo130_assertion description "[A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP95965.RAp0fQZZJOZ9JMuVtixmP_qfyfgNuWe6hvLpVTWohXCAo130_provenance.
NP95967.RAuW1YS10ZnDo8CAP-KBtwD9CVEnEqqvkblVDC7axzQfo130_assertion description "[A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP95967.RAuW1YS10ZnDo8CAP-KBtwD9CVEnEqqvkblVDC7axzQfo130_provenance.
NP95968.RAjDBqAEgXfAIqKifKI-1vjxTodYwgNbm9KJqUQNa4Zps130_assertion description "[A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP95968.RAjDBqAEgXfAIqKifKI-1vjxTodYwgNbm9KJqUQNa4Zps130_provenance.
NP95971.RAro5r2B812qOPHuo7dXgKCtXIUGsvVHzGYq4BfQb9KkQ130_assertion description "[Common variants on 14q32 and 13q12 are associated with DLBCL susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP95971.RAro5r2B812qOPHuo7dXgKCtXIUGsvVHzGYq4BfQb9KkQ130_provenance.
NP95977.RAt1D9H6_L7wrFekYx16chOwPXsrYFylG6rg26NKfbO8A130_assertion description "[Genome-wide meta-analysis identifies regions on 7p21 (AHR) and 15q24 (CYP1A2) as determinants of habitual caffeine consumption.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP95977.RAt1D9H6_L7wrFekYx16chOwPXsrYFylG6rg26NKfbO8A130_provenance.
NP95987.RAg3WWx9Z7vpuu-hCl-kjPBfHJ6o9_gSjkA3bnz2jbXsA130_assertion description "[Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP95987.RAg3WWx9Z7vpuu-hCl-kjPBfHJ6o9_gSjkA3bnz2jbXsA130_provenance.
NP95988.RAnJIehYHG0g_mSk-f8WlEyW8lPOJ43PzQbAuW8J-f7Hg130_assertion description "[Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP95988.RAnJIehYHG0g_mSk-f8WlEyW8lPOJ43PzQbAuW8J-f7Hg130_provenance.
NP95993.RAn1PvyxrJ2yd3rIHFuHW1ufJTjQckcKuc8i4qE7WSGWg130_assertion description "[Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP95993.RAn1PvyxrJ2yd3rIHFuHW1ufJTjQckcKuc8i4qE7WSGWg130_provenance.
NP95995.RAvKSaYO5GfteqS9Wgzjy0s4POzjkCXxxrkx4G1_wdcN8130_assertion description "[Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP95995.RAvKSaYO5GfteqS9Wgzjy0s4POzjkCXxxrkx4G1_wdcN8130_provenance.
NP95996.RAp9sei1gxEHOQEFXNVZ76WGSTghumVljFmhOIemPi0jk130_assertion description "[Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP95996.RAp9sei1gxEHOQEFXNVZ76WGSTghumVljFmhOIemPi0jk130_provenance.
NP96003.RAmV4sxcHkide27bZBVYq9LBQp1WslB9u7A9JprLPrJgQ130_assertion description "[Genome-wide association study identifies a common variant associated with risk of endometrial cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96003.RAmV4sxcHkide27bZBVYq9LBQp1WslB9u7A9JprLPrJgQ130_provenance.
NP96010.RAsGkY3KaGBDxc7cZk4EN3Tqzaq31_vUvBehqa_thVPS4130_assertion description "[These observations suggest a potential unsuspected pathway of host genetic influence on the dynamics of AIDS progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96010.RAsGkY3KaGBDxc7cZk4EN3Tqzaq31_vUvBehqa_thVPS4130_provenance.
NP96014.RAq-emYhhGWL6HoXv0EGY_8Tk6XgrbaOD_89vR1QE1mxQ130_assertion description "[The human AIRE gene at chromosome 21q22 is a genetic determinant for the predisposition to rheumatoid arthritis in Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96014.RAq-emYhhGWL6HoXv0EGY_8Tk6XgrbaOD_89vR1QE1mxQ130_provenance.
NP96020.RAjwKxxQ0JsjaCvZ_0yxV5cQEi5TLoFIw8wkoYOm9D0qs130_assertion description "[We conclude that 1) meta-analyses of consumption data may contribute usefully to gene discovery; 2) translation of human alcoholism GWAS results to drug discovery or clinically useful prediction of risk will be challenging; and 3) through accumulation across studies, GWAS data may become valuable for improved genetic risk differentiation in research in biological psychiatry (e.g., prospective high-risk or resilience studies).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96020.RAjwKxxQ0JsjaCvZ_0yxV5cQEi5TLoFIw8wkoYOm9D0qs130_provenance.
NP96022.RArLaG-bmhm-RXPjfzlR6SMJ3vDkodU06nsrb7DBpBHL4130_assertion description "[We conclude that 1) meta-analyses of consumption data may contribute usefully to gene discovery; 2) translation of human alcoholism GWAS results to drug discovery or clinically useful prediction of risk will be challenging; and 3) through accumulation across studies, GWAS data may become valuable for improved genetic risk differentiation in research in biological psychiatry (e.g., prospective high-risk or resilience studies).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96022.RArLaG-bmhm-RXPjfzlR6SMJ3vDkodU06nsrb7DBpBHL4130_provenance.
NP96023.RAg53rxtxBFQSkIwoBiUgImznw1r2wX1xJevq8QH2lEfk130_assertion description "[We conclude that 1) meta-analyses of consumption data may contribute usefully to gene discovery; 2) translation of human alcoholism GWAS results to drug discovery or clinically useful prediction of risk will be challenging; and 3) through accumulation across studies, GWAS data may become valuable for improved genetic risk differentiation in research in biological psychiatry (e.g., prospective high-risk or resilience studies).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96023.RAg53rxtxBFQSkIwoBiUgImznw1r2wX1xJevq8QH2lEfk130_provenance.
NP96026.RAhTaOaMilfCXvwzj2hrvA--yoOAeMaCnYI8yiw8kiuGA130_assertion description "[We conclude that 1) meta-analyses of consumption data may contribute usefully to gene discovery; 2) translation of human alcoholism GWAS results to drug discovery or clinically useful prediction of risk will be challenging; and 3) through accumulation across studies, GWAS data may become valuable for improved genetic risk differentiation in research in biological psychiatry (e.g., prospective high-risk or resilience studies).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96026.RAhTaOaMilfCXvwzj2hrvA--yoOAeMaCnYI8yiw8kiuGA130_provenance.
NP96027.RAh4uFR-Ss2KDyN-5XGOblOD9NmyCSHxDLZL3OUWdwThA130_assertion description "[We conclude that 1) meta-analyses of consumption data may contribute usefully to gene discovery; 2) translation of human alcoholism GWAS results to drug discovery or clinically useful prediction of risk will be challenging; and 3) through accumulation across studies, GWAS data may become valuable for improved genetic risk differentiation in research in biological psychiatry (e.g., prospective high-risk or resilience studies).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96027.RAh4uFR-Ss2KDyN-5XGOblOD9NmyCSHxDLZL3OUWdwThA130_provenance.
NP96031.RAoR3NYc4SITB0Bcc_WZOZEqTJWPSzj4OrASz-Uw6aThA130_assertion description "[We conclude that 1) meta-analyses of consumption data may contribute usefully to gene discovery; 2) translation of human alcoholism GWAS results to drug discovery or clinically useful prediction of risk will be challenging; and 3) through accumulation across studies, GWAS data may become valuable for improved genetic risk differentiation in research in biological psychiatry (e.g., prospective high-risk or resilience studies).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96031.RAoR3NYc4SITB0Bcc_WZOZEqTJWPSzj4OrASz-Uw6aThA130_provenance.
NP96032.RAl6NJUu2vwnxPi1UE9FHJ_53SXPvwgfsHI0MRrd3kiKU130_assertion description "[We conclude that 1) meta-analyses of consumption data may contribute usefully to gene discovery; 2) translation of human alcoholism GWAS results to drug discovery or clinically useful prediction of risk will be challenging; and 3) through accumulation across studies, GWAS data may become valuable for improved genetic risk differentiation in research in biological psychiatry (e.g., prospective high-risk or resilience studies).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96032.RAl6NJUu2vwnxPi1UE9FHJ_53SXPvwgfsHI0MRrd3kiKU130_provenance.
NP96035.RAvTnC_g_5f1CjezwOGe42ffYz0qOZbtdehnvMwuRvFPU130_assertion description "[Chromosome 7p11.2 (EGFR) variation influences glioma risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96035.RAvTnC_g_5f1CjezwOGe42ffYz0qOZbtdehnvMwuRvFPU130_provenance.
NP96036.RApSzGRM1CddcaOqby90_DnUsseS_jcTT3_buphBHxQwI130_assertion description "[Chromosome 7p11.2 (EGFR) variation influences glioma risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96036.RApSzGRM1CddcaOqby90_DnUsseS_jcTT3_buphBHxQwI130_provenance.
NP96037.RApSa6U6g5j9PftmpsI3IcsE8Cewn1U7YxIMsHQvo_7gw130_assertion description "[Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96037.RApSa6U6g5j9PftmpsI3IcsE8Cewn1U7YxIMsHQvo_7gw130_provenance.
NP96039.RAiDVQVx7pQOhg2QkLruZkw6_ms3WjIGbIQ4T7OSvNaXM130_assertion description "[Genetic variation may modify the risk of death on dialysis. SNPs in proximity to genes regulating vascular extracellular matrix, cardiac ventricular repolarization, and smoking cessation are associated with dialysis survival in AAs with T2D. These results warrant replication in other cohorts and races.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96039.RAiDVQVx7pQOhg2QkLruZkw6_ms3WjIGbIQ4T7OSvNaXM130_provenance.
NP96042.RAgPOSSygkEBMIHzhBVjUx0Ly5fh5Wr3IXAIb38Wu-8p8130_assertion description "[Genetic variation may modify the risk of death on dialysis. SNPs in proximity to genes regulating vascular extracellular matrix, cardiac ventricular repolarization, and smoking cessation are associated with dialysis survival in AAs with T2D. These results warrant replication in other cohorts and races.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96042.RAgPOSSygkEBMIHzhBVjUx0Ly5fh5Wr3IXAIb38Wu-8p8130_provenance.
NP96043.RAkpKMEEGPg-yppz309_Sz2YQHahb1ijyXlWmzIq_cKH8130_assertion description "[Genetic variation may modify the risk of death on dialysis. SNPs in proximity to genes regulating vascular extracellular matrix, cardiac ventricular repolarization, and smoking cessation are associated with dialysis survival in AAs with T2D. These results warrant replication in other cohorts and races.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96043.RAkpKMEEGPg-yppz309_Sz2YQHahb1ijyXlWmzIq_cKH8130_provenance.
NP96045.RAoVeSthQti-VOc-XCiI9HtteJ8Ji6bycl_ETYvn3buLo130_assertion description "[Genetic variation may modify the risk of death on dialysis. SNPs in proximity to genes regulating vascular extracellular matrix, cardiac ventricular repolarization, and smoking cessation are associated with dialysis survival in AAs with T2D. These results warrant replication in other cohorts and races.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96045.RAoVeSthQti-VOc-XCiI9HtteJ8Ji6bycl_ETYvn3buLo130_provenance.
NP96049.RAvrYJ6_xkU4I7ePp-HjwE5wngCjIHOhnQ2mQkXcKXR-c130_assertion description "[Genetic variation may modify the risk of death on dialysis. SNPs in proximity to genes regulating vascular extracellular matrix, cardiac ventricular repolarization, and smoking cessation are associated with dialysis survival in AAs with T2D. These results warrant replication in other cohorts and races.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96049.RAvrYJ6_xkU4I7ePp-HjwE5wngCjIHOhnQ2mQkXcKXR-c130_provenance.
NP96060.RAnncd1XpqzLd9MZgv0JE4fmuFtWLB7aILTbzWqUgKYow130_assertion description "[Genetic variation may modify the risk of death on dialysis. SNPs in proximity to genes regulating vascular extracellular matrix, cardiac ventricular repolarization, and smoking cessation are associated with dialysis survival in AAs with T2D. These results warrant replication in other cohorts and races.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96060.RAnncd1XpqzLd9MZgv0JE4fmuFtWLB7aILTbzWqUgKYow130_provenance.
NP96061.RAlztzUidfauryb1EZax3NIaRK8y9pOr4ljYeiajle_ao130_assertion description "[Genetic variation may modify the risk of death on dialysis. SNPs in proximity to genes regulating vascular extracellular matrix, cardiac ventricular repolarization, and smoking cessation are associated with dialysis survival in AAs with T2D. These results warrant replication in other cohorts and races.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96061.RAlztzUidfauryb1EZax3NIaRK8y9pOr4ljYeiajle_ao130_provenance.
NP96064.RAlXuh0yg-_zJw0b1kkMIKs24hmQvI4X2IVJ__WVsOGmY130_assertion description "[A genome-wide association study on obesity and obesity-related traits.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96064.RAlXuh0yg-_zJw0b1kkMIKs24hmQvI4X2IVJ__WVsOGmY130_provenance.
NP96066.RAop9uDwqX0vSfhb6xCVyvmSvj-f2XYjd4R19FCOEGbgs130_assertion description "[A genome-wide association study on obesity and obesity-related traits.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96066.RAop9uDwqX0vSfhb6xCVyvmSvj-f2XYjd4R19FCOEGbgs130_provenance.
NP96069.RAsbvtt89YZoZXUA7jwsLwWz61x_OklVP5RzafhJ0oUcY130_assertion description "[A genome-wide association study on obesity and obesity-related traits.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96069.RAsbvtt89YZoZXUA7jwsLwWz61x_OklVP5RzafhJ0oUcY130_provenance.
NP96074.RAucv2Idvut6Np8O97EZBEByDNZW5jCxqGjJbT_5l9cSU130_assertion description "[A genome-wide association study on obesity and obesity-related traits.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96074.RAucv2Idvut6Np8O97EZBEByDNZW5jCxqGjJbT_5l9cSU130_provenance.
NP96075.RAukcva5xST3vJz4LXHFItufZidGNyJrzK4XuUksS8M-Q130_assertion description "[Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96075.RAukcva5xST3vJz4LXHFItufZidGNyJrzK4XuUksS8M-Q130_provenance.
NP96077.RAlXLIGHZ_LNnTkwpDwBMGmW44YGArSSZf5wW1MO3SMfk130_assertion description "[Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96077.RAlXLIGHZ_LNnTkwpDwBMGmW44YGArSSZf5wW1MO3SMfk130_provenance.
NP96085.RAt7g5EMF_VGbH987N2m2aVcVkIjQNecNsUn65fFsgbrM130_assertion description "[Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96085.RAt7g5EMF_VGbH987N2m2aVcVkIjQNecNsUn65fFsgbrM130_provenance.
NP96086.RAkfN_irGfgLxw6Eq0kPgXpuYcY43YTDG0iLEmRWlXekQ130_assertion description "[Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96086.RAkfN_irGfgLxw6Eq0kPgXpuYcY43YTDG0iLEmRWlXekQ130_provenance.
NP96087.RAl2SxO7HTaI3i4moeaL6G8QRVMSpBNaI8wBfgpmLz1tI130_assertion description "[Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96087.RAl2SxO7HTaI3i4moeaL6G8QRVMSpBNaI8wBfgpmLz1tI130_provenance.
NP96088.RAg9ulAkAQXlmaFyXq8uqlMsKAbTogmT3RLxHY7QYtFhU130_assertion description "[Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96088.RAg9ulAkAQXlmaFyXq8uqlMsKAbTogmT3RLxHY7QYtFhU130_provenance.
NP96090.RAjJlQuxOsfqVnl96dSSmM5HS0IR99zKTJt13MJCUw4-Y130_assertion description "[Genome-wide association study of prostate cancer in men of African ancestry identifies a susceptibility locus at 17q21.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96090.RAjJlQuxOsfqVnl96dSSmM5HS0IR99zKTJt13MJCUw4-Y130_provenance.
NP96092.RAoxJy2l6pBsvUi6Bc4BDYyJ8HrajQ7EG4NB5KdgnWaOA130_assertion description "[The use of data on genetic variants and the addition of data on global monocytic gene expression led to the identification of the novel functional CAD susceptibility locus LIPA, located on chromosome 10q23.31. The respective eSNPs associated with CAD strongly affect LIPA gene expression level, which was related to endothelial dysfunction, a precursor of CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96092.RAoxJy2l6pBsvUi6Bc4BDYyJ8HrajQ7EG4NB5KdgnWaOA130_provenance.
NP96095.RAlKRKPOUJBssQSNehCJLsK3hGTCpE4IloKkHMlL88h2Y130_assertion description "[These results provide genetic basis for gender differences in MDD and will serve as a resource for replication in other populations to elucidate the potential role of these genetic variants in MDD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96095.RAlKRKPOUJBssQSNehCJLsK3hGTCpE4IloKkHMlL88h2Y130_provenance.
NP96099.RAhQ0dAMMvaKLM2L5fX89v6JwZEXW5eyYIWlneDXHNLlc130_assertion description "[Genome-wide association identifies three new susceptibility loci for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96099.RAhQ0dAMMvaKLM2L5fX89v6JwZEXW5eyYIWlneDXHNLlc130_provenance.
NP96100.RAptwkKdEJVfVugdEwXsyIzZiRMXt8SVsvtLk6GGdYasQ130_assertion description "[We previously identified variants at the CSF1, OPTN and TNFRSF11A loci as risk factors for PDB by genome-wide association study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96100.RAptwkKdEJVfVugdEwXsyIzZiRMXt8SVsvtLk6GGdYasQ130_provenance.
NP96101.RAruIcd9whM5YwyKWzGXeXdICr9JO7QQeyntsVF3szTFY130_assertion description "[Our data also confirmed the association of TM7SF4 (rs2458413, OR = 1.40, P = 7.38 10(-17)) with PDB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96101.RAruIcd9whM5YwyKWzGXeXdICr9JO7QQeyntsVF3szTFY130_provenance.
NP96108.RAqKgpU3fD1QwO_BRIhi5DonU-Ky_BZzQ28Sbb0F77QKE130_assertion description "[Genome-wide association identifies three new susceptibility loci for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96108.RAqKgpU3fD1QwO_BRIhi5DonU-Ky_BZzQ28Sbb0F77QKE130_provenance.
NP96111.RAnkN1kgaq2K4glwTEQi9Bnq-t3UiwD-OyrwlBGYS53n4130_assertion description "[Genome-wide association identifies three new susceptibility loci for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96111.RAnkN1kgaq2K4glwTEQi9Bnq-t3UiwD-OyrwlBGYS53n4130_provenance.
NP96112.RArRcDVM0sj6jv6mlRZ1d1Qsdv2-Dmrax73lTwOZdUNrI130_assertion description "[Genome-wide association identifies three new susceptibility loci for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96112.RArRcDVM0sj6jv6mlRZ1d1Qsdv2-Dmrax73lTwOZdUNrI130_provenance.
NP96115.RAhtSevcBUJqy8SppaDy1bSYVt9QJNdv9DRPaqSiGdSDw130_assertion description "[Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96115.RAhtSevcBUJqy8SppaDy1bSYVt9QJNdv9DRPaqSiGdSDw130_provenance.
NP96125.RApjhSKzIWPVvz-ZBjK3KK7FLD8gpP_DWCx3DtVGN9tjw130_assertion description "[the genetic architecture of disease severity is likely polygenic and comprised of modest effects, similar to what has been described for MS susceptibility, to date.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96125.RApjhSKzIWPVvz-ZBjK3KK7FLD8gpP_DWCx3DtVGN9tjw130_provenance.
NP96129.RAjIADrTqMTyE994hZ5OAWbQr4HoOLpMEjM9kj8wHbNIc130_assertion description "[We demonstrate 11 gene associations for sudden cardiac arrest due to ventricular tachycardia/ventricular fibrillation in patients with coronary artery disease. Validation studies in independent cohorts and functional studies are required to confirm these associations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96129.RAjIADrTqMTyE994hZ5OAWbQr4HoOLpMEjM9kj8wHbNIc130_provenance.
NP96133.RAsxxG4a3OaVLToK5bNoBc9sYlrnFKFwYC9YVlnzo0dcM130_assertion description "[We demonstrate 11 gene associations for sudden cardiac arrest due to ventricular tachycardia/ventricular fibrillation in patients with coronary artery disease. Validation studies in independent cohorts and functional studies are required to confirm these associations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96133.RAsxxG4a3OaVLToK5bNoBc9sYlrnFKFwYC9YVlnzo0dcM130_provenance.
NP96137.RAvFvA4HIebl17_sJTZEet5J73gsVSeWnZTMSEpfVIRuo130_assertion description "[We demonstrate 11 gene associations for sudden cardiac arrest due to ventricular tachycardia/ventricular fibrillation in patients with coronary artery disease. Validation studies in independent cohorts and functional studies are required to confirm these associations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96137.RAvFvA4HIebl17_sJTZEet5J73gsVSeWnZTMSEpfVIRuo130_provenance.
NP96141.RAoBWtFQW37iYt9WnMfwkZMoPdHMoUJY_OiFlBPagZLfA130_assertion description "[We demonstrate 11 gene associations for sudden cardiac arrest due to ventricular tachycardia/ventricular fibrillation in patients with coronary artery disease. Validation studies in independent cohorts and functional studies are required to confirm these associations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96141.RAoBWtFQW37iYt9WnMfwkZMoPdHMoUJY_OiFlBPagZLfA130_provenance.
NP96148.RAh2Z5evfUiGEQrTVuygHthyTYuru6NUejv-kVdkpA8qk130_assertion description "[We demonstrate 11 gene associations for sudden cardiac arrest due to ventricular tachycardia/ventricular fibrillation in patients with coronary artery disease. Validation studies in independent cohorts and functional studies are required to confirm these associations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96148.RAh2Z5evfUiGEQrTVuygHthyTYuru6NUejv-kVdkpA8qk130_provenance.
NP96150.RAsnd2rgqMMn6UV189mpS6zjaR1UYm_SC2rnyAH_wVoSM130_assertion description "[We demonstrate 11 gene associations for sudden cardiac arrest due to ventricular tachycardia/ventricular fibrillation in patients with coronary artery disease. Validation studies in independent cohorts and functional studies are required to confirm these associations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96150.RAsnd2rgqMMn6UV189mpS6zjaR1UYm_SC2rnyAH_wVoSM130_provenance.
NP96153.RAusOHv1YwilgQnIsa4tTGoyXtt3dx22MzUqDfVLEvyPA130_assertion description "[We demonstrate 11 gene associations for sudden cardiac arrest due to ventricular tachycardia/ventricular fibrillation in patients with coronary artery disease. Validation studies in independent cohorts and functional studies are required to confirm these associations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96153.RAusOHv1YwilgQnIsa4tTGoyXtt3dx22MzUqDfVLEvyPA130_provenance.
NP96154.RAtVjwfzDbqW8W67VwtogGO4ppLdZaxLb03K7Pqj14IjM130_assertion description "[We demonstrate 11 gene associations for sudden cardiac arrest due to ventricular tachycardia/ventricular fibrillation in patients with coronary artery disease. Validation studies in independent cohorts and functional studies are required to confirm these associations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96154.RAtVjwfzDbqW8W67VwtogGO4ppLdZaxLb03K7Pqj14IjM130_provenance.
NP96158.RAhdDhpdCbWJg8ah8ukm8EXi8vHpdpJ6N7YaMMG1y_QwE130_assertion description "[We demonstrate 11 gene associations for sudden cardiac arrest due to ventricular tachycardia/ventricular fibrillation in patients with coronary artery disease. Validation studies in independent cohorts and functional studies are required to confirm these associations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96158.RAhdDhpdCbWJg8ah8ukm8EXi8vHpdpJ6N7YaMMG1y_QwE130_provenance.
NP96160.RAheWTiyPdMnv-u8rkPD59oMjzIfrHaA-Zq2vMmtLfyLo130_assertion description "[We demonstrate 11 gene associations for sudden cardiac arrest due to ventricular tachycardia/ventricular fibrillation in patients with coronary artery disease. Validation studies in independent cohorts and functional studies are required to confirm these associations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96160.RAheWTiyPdMnv-u8rkPD59oMjzIfrHaA-Zq2vMmtLfyLo130_provenance.
NP96162.RAptY6d74btpC0XHUv1fAysvlF0LtWeDCNoQM_Ll4PMs8130_assertion description "[We demonstrate 11 gene associations for sudden cardiac arrest due to ventricular tachycardia/ventricular fibrillation in patients with coronary artery disease. Validation studies in independent cohorts and functional studies are required to confirm these associations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96162.RAptY6d74btpC0XHUv1fAysvlF0LtWeDCNoQM_Ll4PMs8130_provenance.
NP96163.RAoXvVqRZiCFvP8-1GL1wuiykiS6eZZzy7cz8pBu3SZe8130_assertion description "[We demonstrate 11 gene associations for sudden cardiac arrest due to ventricular tachycardia/ventricular fibrillation in patients with coronary artery disease. Validation studies in independent cohorts and functional studies are required to confirm these associations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96163.RAoXvVqRZiCFvP8-1GL1wuiykiS6eZZzy7cz8pBu3SZe8130_provenance.
NP96170.RAv_OtMLDK5jlpkt-TAEJa6C6L-SU-GEMsByXiX5i2C0Q130_assertion description "[We demonstrate 11 gene associations for sudden cardiac arrest due to ventricular tachycardia/ventricular fibrillation in patients with coronary artery disease. Validation studies in independent cohorts and functional studies are required to confirm these associations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96170.RAv_OtMLDK5jlpkt-TAEJa6C6L-SU-GEMsByXiX5i2C0Q130_provenance.
NP96182.RAtPYh6NXaIDOo9Sp5haKmc1XdaCDpWtrNUfhJNxCH4_s130_assertion description "[Our findings provide evidence that genetic variation is a determinant of progression-free survival of patients with chronic lymphocytic leukemia. Specific associations warrant further analyses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96182.RAtPYh6NXaIDOo9Sp5haKmc1XdaCDpWtrNUfhJNxCH4_s130_provenance.
NP96188.RAhnYg3vnWwXb7BJz6PCSsPBnuo2Ev5D-umyTUaVLfna8130_assertion description "[TRPM8 has been the focus of neuropathic pain models, whereas LRP1 modulates neuronal glutamate signaling, plausibly linking both genes to migraine pathophysiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96188.RAhnYg3vnWwXb7BJz6PCSsPBnuo2Ev5D-umyTUaVLfna8130_provenance.
NP96190.RApWfPg4p7OAxtp8OSvc9nyvIbyPKWRoEaa8Sv0kckoiY130_assertion description "[TRPM8 has been the focus of neuropathic pain models, whereas LRP1 modulates neuronal glutamate signaling, plausibly linking both genes to migraine pathophysiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96190.RApWfPg4p7OAxtp8OSvc9nyvIbyPKWRoEaa8Sv0kckoiY130_provenance.
NP96193.RAqiYlcz8Id8ySN3xTwZBlwiroWo-hyoMH79F2iT5SULI130_assertion description "[A genome-wide association study of DSM-IV cannabis dependence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96193.RAqiYlcz8Id8ySN3xTwZBlwiroWo-hyoMH79F2iT5SULI130_provenance.
NP96208.RAq2KEQW49oo1u1R1tjcTXpTO4cNAhIbWtwDiHxdazR4M130_assertion description "[The authors identified two candidate regions associated with age at smoking initiation in patients with COPD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96208.RAq2KEQW49oo1u1R1tjcTXpTO4cNAhIbWtwDiHxdazR4M130_provenance.
NP96216.RAqFBbDZxjhSaLtFGZ49TviRUh5tKZlzEnj-9vWR9UgLA130_assertion description "[Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96216.RAqFBbDZxjhSaLtFGZ49TviRUh5tKZlzEnj-9vWR9UgLA130_provenance.
NP96225.RAvmgfYexRQHcr6Ys6tbNAXoYSCM2ihoVbA2YcFr-bgM8130_assertion description "[A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96225.RAvmgfYexRQHcr6Ys6tbNAXoYSCM2ihoVbA2YcFr-bgM8130_provenance.
NP96227.RAsKMnxvNeDh4ABkCmAF38M6f0Totmv-XO5soRxAzDtNc130_assertion description "[A genome-wide association study identifies two new lung cancer susceptibility loci at 13q12.12 and 22q12.2 in Han Chinese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96227.RAsKMnxvNeDh4ABkCmAF38M6f0Totmv-XO5soRxAzDtNc130_provenance.
NP96229.RAlPTiS_S9eTFQUmkbKVIfCX2thuhq0LUrqPfECc26_vI130_assertion description "[Variation in the DEPDC5 locus is associated with progression to hepatocellular carcinoma in chronic hepatitis C virus carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96229.RAlPTiS_S9eTFQUmkbKVIfCX2thuhq0LUrqPfECc26_vI130_provenance.
NP96235.RAgqgBAtbZJZ8fpVLRGeO_zG0l7xi5gRiFSyDbmu46D2c130_assertion description "[This study implicates nine different loci involved in genetic susceptibility to Dupuytrens disease. The fact that six of these nine loci harbor genes encoding proteins in the Wnt-signaling pathway suggests that aberrations in this pathway are key to the process of fibromatosis in Dupuytrens disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96235.RAgqgBAtbZJZ8fpVLRGeO_zG0l7xi5gRiFSyDbmu46D2c130_provenance.
NP96240.RAi2vb5De74SGB1UwFugpTRGUrkNiJwd07jGgYd7vCPrM130_assertion description "[This study implicates nine different loci involved in genetic susceptibility to Dupuytrens disease. The fact that six of these nine loci harbor genes encoding proteins in the Wnt-signaling pathway suggests that aberrations in this pathway are key to the process of fibromatosis in Dupuytrens disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96240.RAi2vb5De74SGB1UwFugpTRGUrkNiJwd07jGgYd7vCPrM130_provenance.
NP96247.RAkOzEz3XbHpW_kC6nJ54C4qeIKMeYlTf-Oikz51_cuX0130_assertion description "[Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96247.RAkOzEz3XbHpW_kC6nJ54C4qeIKMeYlTf-Oikz51_cuX0130_provenance.
NP96257.RAjwYlf8Ucve6G7xzlZJep8aKlc7Tx3KgfVYS-mUX4gBM130_assertion description "[Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96257.RAjwYlf8Ucve6G7xzlZJep8aKlc7Tx3KgfVYS-mUX4gBM130_provenance.
NP96258.RApatvevHMRuTuprHlMt9VdNC_CHP1J4UzvzcXe6xnQZM130_assertion description "[Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96258.RApatvevHMRuTuprHlMt9VdNC_CHP1J4UzvzcXe6xnQZM130_provenance.
NP96259.RAvt4dtMXj0CunEwVQgFFy3zIbQ1yI9VUWcYBuLqtSF1w130_assertion description "[Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96259.RAvt4dtMXj0CunEwVQgFFy3zIbQ1yI9VUWcYBuLqtSF1w130_provenance.
NP96262.RArG9X9h041KcumfCQAfVEKSorQgwdXpwYFPAarHrTUc0130_assertion description "[Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96262.RArG9X9h041KcumfCQAfVEKSorQgwdXpwYFPAarHrTUc0130_provenance.
NP96263.RAuxPQyzdvTu2zD471NRc2uNippJlUPh1cxi7mDIczpmQ130_assertion description "[Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96263.RAuxPQyzdvTu2zD471NRc2uNippJlUPh1cxi7mDIczpmQ130_provenance.
NP96266.RAuZah6ZQRXF09JEYwBtXsVQg3IRqUtkB6kwPx80Gt25Q130_assertion description "[Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96266.RAuZah6ZQRXF09JEYwBtXsVQg3IRqUtkB6kwPx80Gt25Q130_provenance.
NP96269.RAuo974foVgqBxMld9nFeuFVwvlIp7BUoxJrtH4ckl4Mg130_assertion description "[Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96269.RAuo974foVgqBxMld9nFeuFVwvlIp7BUoxJrtH4ckl4Mg130_provenance.
NP96272.RAtQTpqSfJA_g-2yJB-x0CzuLsfBibCpesaZYMv3dCVt8130_assertion description "[A genome-wide association study of bladder cancer identifies a new susceptibility locus within SLC14A1, a urea transporter gene on chromosome 18q12.3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96272.RAtQTpqSfJA_g-2yJB-x0CzuLsfBibCpesaZYMv3dCVt8130_provenance.
NP96276.RAp3EoqT2sHBfI7q4udaACg76hv76pCknSTSbn5JKUiYA130_assertion description "[Follow-up of the 17 top SNPs in an independent sample of 1,682 SSc and 3,926 controls showed associations at PSORS1C1 (overall P=5.7010(-10), OR:1.25), TNIP1 (P=4.6810(-9), OR:1.31), and RHOB loci (P=3.1710(-6), OR:1.21).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96276.RAp3EoqT2sHBfI7q4udaACg76hv76pCknSTSbn5JKUiYA130_provenance.
NP96283.RAvEz0pHYBf4ExrPRIusf_4b2SQvwW55EIgSAOKW0EkC0130_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." NP96283.RAvEz0pHYBf4ExrPRIusf_4b2SQvwW55EIgSAOKW0EkC0130_provenance.
NP96284.RAhHbVoPjhQehe8MyTYyDZ03R9uTf5nAFou_pqgO75pGo130_assertion description "[, we identified and replicated one novel locus in association with serum urate levels and experimentally characterize the novel G65W variant in URAT1 as a functional allele.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96284.RAhHbVoPjhQehe8MyTYyDZ03R9uTf5nAFou_pqgO75pGo130_provenance.
NP96295.RAp5CdluhTf1mm25asiNv2UUh0AGdEc9s52wl9-DF8Oqw130_assertion description "[Within the HLA region, HLA-DQB1, HLA-DPA1/B1, and NOTCH4 associations with SSc are likely confined to specific auto-antibodies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96295.RAp5CdluhTf1mm25asiNv2UUh0AGdEc9s52wl9-DF8Oqw130_provenance.
NP96297.RAsAX8u9WKnr6hj44WydLeMfMBDqwOh2IbtJ-w0159ddI130_assertion description "[Overall analysis showed that non-HLA polymorphism rs11642873 in IRF8 gene to be associated at GWAS level with lcSSc (P=2.3210(-12), OR=0.75).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96297.RAsAX8u9WKnr6hj44WydLeMfMBDqwOh2IbtJ-w0159ddI130_provenance.

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