Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP91885.RAuJMRhAIrvf8Kgw_vMhVfdQvU0vuEGvS_T8BUAOMADfY130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP91885.RAuJMRhAIrvf8Kgw_vMhVfdQvU0vuEGvS_T8BUAOMADfY130_provenance.
- NP91890.RAlDuF5n0RP9DozHqTtP0DqhXKXXHxvlxCJKQOmAE2cr4130_assertion description "[An approach based on a genome-wide association study reveals candidate loci for narcolepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP91890.RAlDuF5n0RP9DozHqTtP0DqhXKXXHxvlxCJKQOmAE2cr4130_provenance.
- NP91894.RArBztPrHOR0_HTzQStKFwGSL2MB-hFQws3pu7fuAadOo130_assertion description "[Common polymorphisms in ITGA2, PON1 and THBS2 are associated with coronary atherosclerosis in a candidate gene association study of the Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP91894.RArBztPrHOR0_HTzQStKFwGSL2MB-hFQws3pu7fuAadOo130_provenance.
- NP91895.RAlZbyOLq2RtSB3GGhaYXS-AhCSvXmMMX30f5SVEO8bTI130_assertion description "[Gene variants associated with venous thrombosis: confirmation in the MEGA study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP91895.RAlZbyOLq2RtSB3GGhaYXS-AhCSvXmMMX30f5SVEO8bTI130_provenance.
- NP91896.RAtuQKR9ShJBpYC7kIJKRTGeYV89AY_1F54Rd8-pkSWT0130_assertion description "[We present an investigation of joint genetic and clinical factors associated with atherosclerosis that shows predictive results for both cases, as well as enhanced performance for their combination.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP91896.RAtuQKR9ShJBpYC7kIJKRTGeYV89AY_1F54Rd8-pkSWT0130_provenance.
- NP91898.RAl4dSSPrQM7haMyttc9-PHbJHOppkPW8PibX6ek2yWKc130_assertion description "[These data do not suggest independent or interactive effects of the TH Val(81)Met, the 5-HTTLPR/rs25531, or the STin2 polymorphisms in BPD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP91898.RAl4dSSPrQM7haMyttc9-PHbJHOppkPW8PibX6ek2yWKc130_provenance.
- NP91900.RAscPTCGswhwndjibXj1OOg4V83Qm0Pwzd6X3cv3JiKNU130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP91900.RAscPTCGswhwndjibXj1OOg4V83Qm0Pwzd6X3cv3JiKNU130_provenance.
- NP91902.RAk0SqwLKLWoetu92burCTBh9D7FSOWx3ItgUhckmhPyg130_assertion description "[Genetic variations in TGFBR3 appear to be associated with a genetic predisposition to development of asthma and to phenotypes of asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP91902.RAk0SqwLKLWoetu92burCTBh9D7FSOWx3ItgUhckmhPyg130_provenance.
- NP91905.RArBgtIckLrivHDTVFezWJNGMfWGyKwzl-HZF03Wyiudg130_assertion description "[SNPs in genes coding for ROS metabolism and signalling in association with docetaxel clearance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP91905.RArBgtIckLrivHDTVFezWJNGMfWGyKwzl-HZF03Wyiudg130_provenance.
- NP91918.RAg27gJxQfh2dfmo_SrHBqcnhh-WX8d-oZF-xc0rgVcps130_assertion description "[Cluster analysis may identify meaningful disease subtypes and/or groups of related phenotypic variables even in a highly selected group of severe emphysema subjects, and may be useful for genetic association studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP91918.RAg27gJxQfh2dfmo_SrHBqcnhh-WX8d-oZF-xc0rgVcps130_provenance.
- NP91920.RAhOXXkfYvz413_3-3qOid_5hSGLLb3EWjVXRpAei5uzM130_assertion description "[These results suggest that CACNA1C may be associated with secondary hyperparathyroidism. In addition, the haplotype-based approach may be useful to screen for key molecules associated with complex traits.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP91920.RAhOXXkfYvz413_3-3qOid_5hSGLLb3EWjVXRpAei5uzM130_provenance.
- NP91926.RAuV86Dzl2nc6s_AcpqSB0kRjVEaEKjLSs_mUEfh-Rzag130_assertion description "[No associations between individual cytokine genetic polymorphisms and susceptibility of KD were observed, but a gene-dosage effect on the risk of KD was found, especially for older or female subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP91926.RAuV86Dzl2nc6s_AcpqSB0kRjVEaEKjLSs_mUEfh-Rzag130_provenance.
- NP91927.RAkkWhRZvZp0FF1gd9HNvc78WaIqbCdBlg8QzOWKjDoCQ130_assertion description "[The results suggest that the TGFB1 gene polymorphism -509C/T may play a potential role in the severity of persistent AR in childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP91927.RAkkWhRZvZp0FF1gd9HNvc78WaIqbCdBlg8QzOWKjDoCQ130_provenance.
- NP91931.RApBgC03yk21V0pswAZDXlw_ifREMGBAYbjA09bfA-5kw130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP91931.RApBgC03yk21V0pswAZDXlw_ifREMGBAYbjA09bfA-5kw130_provenance.
- NP91934.RAk6q59qgqOAMqLCM0H2sFPaoSi54jLhUBtltgMifLn2A130_assertion description "[The frequency of the G allele at the position 210 of the TFRC gene was significantly higher in T2D patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP91934.RAk6q59qgqOAMqLCM0H2sFPaoSi54jLhUBtltgMifLn2A130_provenance.
- NP91940.RAhcU-j_Kq3Q176b9iFNWS3msUSCUoJhrRuTucJ6fBekI130_assertion description "[The results of our study indicate that genetic variation of F2 is associated with kidney stone risk in Northeastern Thai female patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP91940.RAhcU-j_Kq3Q176b9iFNWS3msUSCUoJhrRuTucJ6fBekI130_provenance.
- NP91941.RAlcMshXKfieNDuvyICeMJczAkcC-bFnRLtafvlrQIVFg130_assertion description "[Association of gene polymorphisms with chronic kidney disease in Japanese individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP91941.RAlcMshXKfieNDuvyICeMJczAkcC-bFnRLtafvlrQIVFg130_provenance.
- NP91945.RAr2UhBME1kGC8XNUWAh8gWuMpW6Fp3ZjEy26CX-tOFB8130_assertion description "[Modest associations were observed in CITED2, EP300, CREBBP, TFAP2A and CARM1 but not ALX1. However, these modest associations were not statistically significant after correction for multiple comparisons. Searching for potential functional variants and rare causal mutations is warranted in these genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP91945.RAr2UhBME1kGC8XNUWAh8gWuMpW6Fp3ZjEy26CX-tOFB8130_provenance.
- NP91946.RAt0-db1JmIpmba8m1yWxTjKC_-yIkip4X_9Qta0EjWIY130_assertion description "[Mitochondrial DNA and TFAM gene variation in early-onset myocardial infarction: evidence for an association to haplogroup H.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP91946.RAt0-db1JmIpmba8m1yWxTjKC_-yIkip4X_9Qta0EjWIY130_provenance.
- NP91949.RAosR7n_26-Y9b0E5cQBJLvEKERL3dq4ZGSa2TJhrpFJQ130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP91949.RAosR7n_26-Y9b0E5cQBJLvEKERL3dq4ZGSa2TJhrpFJQ130_provenance.
- NP91954.RAqLDmI0s6PpNWV63WUnmWa261_XsfyGE28QeAxCCATZY130_assertion description "[This is the first study to report that rare hTERT VNTRs are associated with prostate cancer predisposition and that the VNTRs can induce enhanced levels of hTERT promoter activity in prostate cancer cell lines. Thus, the hTERT-VNTR2-2nd locus may function as a modifier of prostate cancer risk by affecting gene expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP91954.RAqLDmI0s6PpNWV63WUnmWa261_XsfyGE28QeAxCCATZY130_provenance.
- NP91963.RAnkdJKfWUlHWnCU7Z76yg-a54Hc24NAhVB-Gzu1kG6dU130_assertion description "[Association between genetic variants in the base excision repair pathway and outcomes after hematopoietic cell transplantations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP91963.RAnkdJKfWUlHWnCU7Z76yg-a54Hc24NAhVB-Gzu1kG6dU130_provenance.
- NP91968.RAqQ-kLoTJI6MQsJYcqyiFw1TH2eeIFeuQcEU1rV_Bbg8130_assertion description "[We present an investigation of joint genetic and clinical factors associated with atherosclerosis that shows predictive results for both cases, as well as enhanced performance for their combination.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP91968.RAqQ-kLoTJI6MQsJYcqyiFw1TH2eeIFeuQcEU1rV_Bbg8130_provenance.
- NP91970.RApmNq-6hJjkCRsKBhTkFVCjAsyLBo6M5_rLD2RK7U9F0130_assertion description "[These data support the hypothesis that alterations in homocysteine metabolism and an unfavorable blood lipoprotein profile may have a common genetic basis. Such conditions may be relevant for studies investigating independent risk factors for vascular disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP91970.RApmNq-6hJjkCRsKBhTkFVCjAsyLBo6M5_rLD2RK7U9F0130_provenance.
- NP91971.RAjHnMANqPrvqvnV7qkwIegsNkl6C5MNzhOOCAspb3ztw130_assertion description "[Long-term follow-up is needed to test associations with metastases and mortality, and the observed genetic effects require replication.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP91971.RAjHnMANqPrvqvnV7qkwIegsNkl6C5MNzhOOCAspb3ztw130_provenance.
- NP91978.RAjVNy4buVKuUmE5BT-d-mKvwUnG2d268FRMBLxU6dvEo130_assertion description "[Variation in TCF7L2 and increased risk of colon cancer: the Atherosclerosis Risk in Communities (ARIC) Study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP91978.RAjVNy4buVKuUmE5BT-d-mKvwUnG2d268FRMBLxU6dvEo130_provenance.
- NP91985.RAvT6RhJit-DjdG7FwqMDcwTun3yIR6L5UO9KW7qCJgzE130_assertion description "[Pathway-based approaches to imaging genetics association studies: Wnt signaling, GSK3beta substrates and major depression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP91985.RAvT6RhJit-DjdG7FwqMDcwTun3yIR6L5UO9KW7qCJgzE130_provenance.
- NP91988.RAt7y8_XYkdim4NIxOEbTcdaxp42jNByMgUhf1C4KaGsI130_assertion description "[HNF1B alterations associated with congenital anomalies of the kidney and urinary tract.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP91988.RAt7y8_XYkdim4NIxOEbTcdaxp42jNByMgUhf1C4KaGsI130_provenance.
- NP92001.RAsVutUFfCZwWzBdRs6YViJf7eCyBhD0XuV2q1fpOUyhk130_assertion description "[An approach based on a genome-wide association study reveals candidate loci for narcolepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92001.RAsVutUFfCZwWzBdRs6YViJf7eCyBhD0XuV2q1fpOUyhk130_provenance.
- NP92003.RApTJ9xC3kT1JLjnNBpS1xs-0TPFmJkRkY3vgrPS2pYGk130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92003.RApTJ9xC3kT1JLjnNBpS1xs-0TPFmJkRkY3vgrPS2pYGk130_provenance.
- NP92004.RAr31l-xf53O7PPr4pMahPBO_XwXiVkNTGS0_C2Mo_mrE130_assertion description "[An approach based on a genome-wide association study reveals candidate loci for narcolepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92004.RAr31l-xf53O7PPr4pMahPBO_XwXiVkNTGS0_C2Mo_mrE130_provenance.
- NP92005.RAr9330TMz8WUybcFOA4zP-er_SLlOnXGkuFdWBrcf4Ew130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92005.RAr9330TMz8WUybcFOA4zP-er_SLlOnXGkuFdWBrcf4Ew130_provenance.
- NP92012.RAsmB2pBePotiDvBpWe9aOw41xrj3QD8ubkrnEKOE1VTg130_assertion description "[These data, coupled with cell and animal model data implicating neuronal signaling in alcohol response, support the conclusion that neuronal signaling is mechanistically involved in alcohols cellular and behavioral effects. Further, these data suggest that genetic variation in these signaling pathways contribute to human variation in alcohol response. Finally, this concordance of the cell, animal, and human findings supports neuronal signaling, particularly glutamate signaling, as a prime target for translational studies to understand and eventually modulate alcohols effects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92012.RAsmB2pBePotiDvBpWe9aOw41xrj3QD8ubkrnEKOE1VTg130_provenance.
- NP92015.RAn1VZY0T8u3yeGdIyXCTMPX1y85w56dB8sup-fSFldTA130_assertion description "[A genome-wide study reveals copy number variants exclusive to childhood obesity cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92015.RAn1VZY0T8u3yeGdIyXCTMPX1y85w56dB8sup-fSFldTA130_provenance.
- NP92022.RAhvFPLedZC6bUfu3zGauvBWG9SD66qeXDnNOvpr4rQiQ130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92022.RAhvFPLedZC6bUfu3zGauvBWG9SD66qeXDnNOvpr4rQiQ130_provenance.
- NP92023.RAkFamsAHigX7VSINWgv2A3RENHxswvWfQL55y7RIYN9g130_assertion description "[A genome-wide scan for common alleles affecting risk for autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92023.RAkFamsAHigX7VSINWgv2A3RENHxswvWfQL55y7RIYN9g130_provenance.
- NP92029.RAtaAUqIei0FGMNitwhWAWbpj3QmJC2jeICaFE27khqDU130_assertion description "[Although we have not been able to found a clear association between the studied CNVs and psychiatric disorders, the rare variants found only within the patients could account for a step further towards understanding the pathophysiology of psychiatric disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92029.RAtaAUqIei0FGMNitwhWAWbpj3QmJC2jeICaFE27khqDU130_provenance.
- NP92039.RAs_AZiRt61VSFBDNpXz-ri3UIFl1xa1l2bFWAN3S9VJ8130_assertion description "[Functional impact of global rare copy number variation in autism spectrum disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92039.RAs_AZiRt61VSFBDNpXz-ri3UIFl1xa1l2bFWAN3S9VJ8130_provenance.
- NP92043.RAvvHjwB4lodEh_NY-R4jzAdcei0Gb4huaiHriAe45h8E130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92043.RAvvHjwB4lodEh_NY-R4jzAdcei0Gb4huaiHriAe45h8E130_provenance.
- NP92046.RAvrbiz3ZmCYcGygjKpjWfxV435xorwcc03HCRIIpHaRk130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92046.RAvrbiz3ZmCYcGygjKpjWfxV435xorwcc03HCRIIpHaRk130_provenance.
- NP92047.RAn_2W0KKe6VVg4fk-JfjpQtjp09cQffY0orKB-qVfQjc130_assertion description "[Evaluation of candidate stromal epithelial cross-talk genes identifies association between risk of serous ovarian cancer and TERT, a cancer susceptibility `hot-spot`.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92047.RAn_2W0KKe6VVg4fk-JfjpQtjp09cQffY0orKB-qVfQjc130_provenance.
- NP92049.RAkO2NTRApcFmvox1nPXF8XVAMLsFfhEiFgEQVK9f6y9Q130_assertion description "[Overall, there is no conclusive evidence that genetic variants in genes involved in the estrogen metabolic pathway are associated with mammographic density in postmenopausal women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92049.RAkO2NTRApcFmvox1nPXF8XVAMLsFfhEiFgEQVK9f6y9Q130_provenance.
- NP92051.RAlTDp58TiRKKfZ-y5leqdr2RDItHkWROi-LNcAHX76wE130_assertion description "[There were significant interactions between SULT1A1*3 and hot flashes (P < 0.001) and between SULT1A1*2 and depressive symptoms (P = 0.007) on menopausal stage, and there were race-specific effects of SULT1A1*2, SULT1A1*3, CYP1B1*3, and CYP3A4*1B on menopause.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92051.RAlTDp58TiRKKfZ-y5leqdr2RDItHkWROi-LNcAHX76wE130_provenance.
- NP92052.RAh5ZUHfCNOWaeOp6NfKGfUyjwLQjaPU5w1rcMzBe-j78130_assertion description "[An approach based on a genome-wide association study reveals candidate loci for narcolepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92052.RAh5ZUHfCNOWaeOp6NfKGfUyjwLQjaPU5w1rcMzBe-j78130_provenance.
- NP92053.RAq_6N11zImHPnkuUzOGNNxYwp_KKMONZvT5xNPtqs2Wk130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92053.RAq_6N11zImHPnkuUzOGNNxYwp_KKMONZvT5xNPtqs2Wk130_provenance.
- NP92054.RAj_hkzuViuBDQIc0TXaZXN5Qdm-UP7y5po0Y3tVXDnNw130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92054.RAj_hkzuViuBDQIc0TXaZXN5Qdm-UP7y5po0Y3tVXDnNw130_provenance.
- NP92055.RAltuZu9MLQ7zgaEopDIUFBYhH60QDhJB-_uBtt75I72Q130_assertion description "[Support Vector Machine based feature selection method in this research found novel association between combinations of SNPs and T2D in a Korean population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92055.RAltuZu9MLQ7zgaEopDIUFBYhH60QDhJB-_uBtt75I72Q130_provenance.
- NP92056.RArNR9JaQiW55fI2o8YZ42ctjZXSU2QXPBbbSmtj5u1Qk130_assertion description "[Despite the relevance of both pathways in the pathogenesis of the disease, and the fact that this is indeed the first study that considers these pathways as a candidate-gene selection approach, our study does not present any evidence of the presence of low-penetrance variants for the selected markers in any of the considered genes in our cohort.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92056.RArNR9JaQiW55fI2o8YZ42ctjZXSU2QXPBbbSmtj5u1Qk130_provenance.
- NP92057.RAu9VXS05zwHqDaslR5NvTr2J9DjWIIvRq7bQACI9Rr1g130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92057.RAu9VXS05zwHqDaslR5NvTr2J9DjWIIvRq7bQACI9Rr1g130_provenance.
- NP92062.RAgO4YsBe6IXJEXOWZ2CWO0rH4UsGviWpsNkyz7_O-3Zs130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92062.RAgO4YsBe6IXJEXOWZ2CWO0rH4UsGviWpsNkyz7_O-3Zs130_provenance.
- NP92066.RAq5mzNE3kpLFd5YVRAWFxbhcaVus-I1ClFX9Rf4Y_dqs130_assertion description "[An approach based on a genome-wide association study reveals candidate loci for narcolepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92066.RAq5mzNE3kpLFd5YVRAWFxbhcaVus-I1ClFX9Rf4Y_dqs130_provenance.
- NP92070.RAgy036IHBfbMBOJwbH7X_6ynDxoiLqGNLiZRZGZ6m1s0130_assertion description "[Centrosome-related genes, genetic variation, and risk of breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92070.RAgy036IHBfbMBOJwbH7X_6ynDxoiLqGNLiZRZGZ6m1s0130_provenance.
- NP92076.RArAtj75xOL4CMnbVhbc2MvOM9Gdl3UtxjNxmW9LcRwIo130_assertion description "[This is the first report on the combined association of CYP1A1 and SULT gene polymorphisms in endometrial cancer that suggests a decreased single nucleotide polymorphism of CYP1A1 and an increased single nucleotide polymorphism for SULT1A1 and SULT1E1 genes may be risk factors for endometrial cancer in Caucasians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92076.RArAtj75xOL4CMnbVhbc2MvOM9Gdl3UtxjNxmW9LcRwIo130_provenance.
- NP92083.RAh_YG4LVdLbQ4gEzJqLETAfAlcPkvvY8LIANgiJkA5_A130_assertion description "[Haplotype analyses identified additional regions of CD28, FCGR2, GATA3, IL2RA, STAT4, and STAT6 associated with childhood ALL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92083.RAh_YG4LVdLbQ4gEzJqLETAfAlcPkvvY8LIANgiJkA5_A130_provenance.
- NP92084.RAtoQBv6dhTrjlfbczjvdTvyRXPkz1WiwOAuLnsQZWGCM130_assertion description "[Comprehensive association analysis of candidate genes for generalized vitiligo supports XBP1, FOXP3, and TSLP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92084.RAtoQBv6dhTrjlfbczjvdTvyRXPkz1WiwOAuLnsQZWGCM130_provenance.
- NP92085.RAmuEBT5QvzTCDJdtqS_CO77eQ5xlgHp9j0pz08TM0s78130_assertion description "[In this cohort of Turkish children with HIES, a majority had normal STAT3, implicating other targets in disease pathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92085.RAmuEBT5QvzTCDJdtqS_CO77eQ5xlgHp9j0pz08TM0s78130_provenance.
- NP92091.RAq-2lh6KNaFl1DBtJqNOqa_jI0twVZMmraOP-hg5kUaU130_assertion description "[Evaluation of candidate stromal epithelial cross-talk genes identifies association between risk of serous ovarian cancer and TERT, a cancer susceptibility `hot-spot`.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92091.RAq-2lh6KNaFl1DBtJqNOqa_jI0twVZMmraOP-hg5kUaU130_provenance.
- NP92097.RAj78_3RMGM6bUInb8-QwuyKTcfqUmE6Jb4sMofUTyZys130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92097.RAj78_3RMGM6bUInb8-QwuyKTcfqUmE6Jb4sMofUTyZys130_provenance.
- NP92105.RAgpVhVWKZgmkwxtUn0dXIvMAoqYLXJUnnYCgqqXFV8NE130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92105.RAgpVhVWKZgmkwxtUn0dXIvMAoqYLXJUnnYCgqqXFV8NE130_provenance.
- NP92106.RAmN-F6U02LBC79u_Wnaya2vTC5bNX9tZjfXvikN13E1k130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92106.RAmN-F6U02LBC79u_Wnaya2vTC5bNX9tZjfXvikN13E1k130_provenance.
- NP92107.RAlQ0V2JAupxNmLiah_eStbzw1p5sFaclRaf1-lsy72Ho130_assertion description "[Evaluation of candidate stromal epithelial cross-talk genes identifies association between risk of serous ovarian cancer and TERT, a cancer susceptibility `hot-spot`.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92107.RAlQ0V2JAupxNmLiah_eStbzw1p5sFaclRaf1-lsy72Ho130_provenance.
- NP92108.RAm_TCH11cItLheERhE5b5PedEy51bFXkXE6wiHH6zPl0130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92108.RAm_TCH11cItLheERhE5b5PedEy51bFXkXE6wiHH6zPl0130_provenance.
- NP92117.RAomsVuxTZrYnzEBfNSuZpGz-akoD6gTySjbvdIWpuqYo130_assertion description "[This trend should be interpreted very carefully. There is also the possibility that other variant of gene in linkage disequilibrium with -48A/G polymorphism was responsible for the trend observed in this study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92117.RAomsVuxTZrYnzEBfNSuZpGz-akoD6gTySjbvdIWpuqYo130_provenance.
- NP92118.RAjlCxBFFkoNS47SZoIdgZaqKId3gBJQ33-Oo45nDnZOc130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92118.RAjlCxBFFkoNS47SZoIdgZaqKId3gBJQ33-Oo45nDnZOc130_provenance.
- NP92120.RApix9lHDopd9EncTvaFHN9dHhPJljvYdIHp8WGV6UJrk130_assertion description "[Our study provides an independent replication of the associations between several SNPs in ZBTB40, ESR1, OPG, RANK, LRP5, and SOST with lumbar spine and/or total hip BMDs in a large sample of Han Chinese women. The results of this study further support the significant associations found between osteoporotic fracture and SNPs in SPTBN1 and SOST. Our results suggest that these variants represent osteoporosis susceptibility genes in both Han Chinese and European populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92120.RApix9lHDopd9EncTvaFHN9dHhPJljvYdIHp8WGV6UJrk130_provenance.
- NP92121.RAtEx5Kv_xG077Na47Nh0TzKw8stIj4g_bO7xUhSTuOwQ130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92121.RAtEx5Kv_xG077Na47Nh0TzKw8stIj4g_bO7xUhSTuOwQ130_provenance.
- NP92124.RApKV1YC_uuRgIjDebdRqDW4JysqrgdliQejf6P_pUiWE130_assertion description "[The difference in population structure partly accounts for some of these significant associations, and the strength of association proved to be sensitive to all levels of sub-structuring whether in the hospital or population-based study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92124.RApKV1YC_uuRgIjDebdRqDW4JysqrgdliQejf6P_pUiWE130_provenance.
- NP92126.RAir8c79x9Un-EPP-JY8c4xOX41RL04QI4ZyIk83Ajf_A130_assertion description "[Evaluation of candidate stromal epithelial cross-talk genes identifies association between risk of serous ovarian cancer and TERT, a cancer susceptibility `hot-spot`.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92126.RAir8c79x9Un-EPP-JY8c4xOX41RL04QI4ZyIk83Ajf_A130_provenance.
- NP92128.RAmu31vHTdgj2kSE18A4vc8Kt_7nCrJZ-ALsQIObiI8Zo130_assertion description "[The -156 delG/G polymorphism of OPN gene could serve as a candidate genetic marker used to evaluate the risk of calcium urolithiasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92128.RAmu31vHTdgj2kSE18A4vc8Kt_7nCrJZ-ALsQIObiI8Zo130_provenance.
- NP92129.RAoPcpUeLDTFdf65fF89DJBdL2Df6mcM3I9bKpgrLrgLs130_assertion description "[Evaluation of candidate stromal epithelial cross-talk genes identifies association between risk of serous ovarian cancer and TERT, a cancer susceptibility `hot-spot`.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92129.RAoPcpUeLDTFdf65fF89DJBdL2Df6mcM3I9bKpgrLrgLs130_provenance.
- NP92131.RAlp6BxECJl61msQ8NOXoBCRSdWORffiOS2hmxnG0RgXo130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92131.RAlp6BxECJl61msQ8NOXoBCRSdWORffiOS2hmxnG0RgXo130_provenance.
- NP92132.RAq0cTUH4JQIWu_VproMO6BdYQXQtiq4ktz-9kCNgugrw130_assertion description "[Osteopontin genotype is a genetic modifier of disease severity in Duchenne dystrophy. Inclusion of genotype data as a covariate or in inclusion criteria in DMD clinical trials would reduce intersubject variance, and increase sensitivity of the trials, particularly in older subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92132.RAq0cTUH4JQIWu_VproMO6BdYQXQtiq4ktz-9kCNgugrw130_provenance.
- NP92139.RAjF5EyM8Gq2aU_fZTbpUHJ89di1N_0ViN1cCLOq664LE130_assertion description "[This study identified new variants of the SPAST gene which included benign missense variants and short insertions/deletions. No large rearrangements were found. Based on these data, 7 new pathogenic variants of HSP are associated with clinical phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92139.RAjF5EyM8Gq2aU_fZTbpUHJ89di1N_0ViN1cCLOq664LE130_provenance.
- NP92140.RAkBs_WJkmOrniGpDonTVx8dmwxGXV8_oU9ZJsBdNZQc8130_assertion description "[Association of gene polymorphisms with chronic kidney disease in Japanese individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92140.RAkBs_WJkmOrniGpDonTVx8dmwxGXV8_oU9ZJsBdNZQc8130_provenance.
- NP92142.RAgK7a3f_yI_-a9nGovoXPV-Kv6jIBC9_2NFJPhlSwMTQ130_assertion description "[Evaluation of candidate stromal epithelial cross-talk genes identifies association between risk of serous ovarian cancer and TERT, a cancer susceptibility `hot-spot`.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92142.RAgK7a3f_yI_-a9nGovoXPV-Kv6jIBC9_2NFJPhlSwMTQ130_provenance.
- NP92143.RAo4uC_O9FAJrGB6d8B4u-85V0lmiA08Aq9eX5k5hoM08130_assertion description "[To investigate the involvement of SPARC (secreted protein acidic and rich in cysteine) mutations and copy number variation in juvenile-onset primary open-angle glaucoma (JPOAG).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92143.RAo4uC_O9FAJrGB6d8B4u-85V0lmiA08Aq9eX5k5hoM08130_provenance.
- NP92147.RAudttHpqPFTpp0BCPWCo0DMBlOSp7phMDto1UabL9sQA130_assertion description "[Analysis of copy number variation in 8,842 Korean individuals reveals 39 genes associated with hepatic biomarkers AST and ALT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92147.RAudttHpqPFTpp0BCPWCo0DMBlOSp7phMDto1UabL9sQA130_provenance.
- NP92151.RAv1RGvVfyllXOF8vY8mtWmNmiWLf68-lF_b7vQLxyXuU130_assertion description "[We confirm that 5 genetic regions associated with lipid traits in European-derived populations are relevant in African Americans. To further evaluate these loci, fine-mapping in larger African American cohorts and/or resequencing will be required.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92151.RAv1RGvVfyllXOF8vY8mtWmNmiWLf68-lF_b7vQLxyXuU130_provenance.
- NP92154.RApGoGa1wvBylLpmgcgyhCnFPZGC36iH2nUps8RzxvwzM130_assertion description "[A genetic risk score based on nine genetic variants independently associated with CAD irrespective of other cardiovascular risk factors was associated with the presence of the disease. Cohort studies are needed to determine whether this genetic risk score can improve the predictive capacity or the risk classification of classical risk functions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92154.RApGoGa1wvBylLpmgcgyhCnFPZGC36iH2nUps8RzxvwzM130_provenance.
- NP92159.RAusN9QU1wYAJ8CeDMsbnn8dPAQfwhl2RfLzU9YTNH910130_assertion description "[We genotyped men with localized/regional prostate cancer for 26 loci across eight genes that are central to cellular antioxidant defence: glutathione peroxidase (GPX1, GPX4), peroxisome proliferator-activated receptor coactivator (PPARGC1A, PPARGC1B), SOD1, SOD2, and SOD3, and 'X-ray repair complementing defective repair in Chinese hamster cell 1' (XRCC1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92159.RAusN9QU1wYAJ8CeDMsbnn8dPAQfwhl2RfLzU9YTNH910130_provenance.
- NP92162.RAreF89FoS919QjlmBp0I_MrNzUBw8vLUUH0RZfjwkjiY130_assertion description "[Inter-individual variation in DNA damage and base excision repair in young, healthy non-smokers: effects of dietary supplementation and genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92162.RAreF89FoS919QjlmBp0I_MrNzUBw8vLUUH0RZfjwkjiY130_provenance.
- NP92167.RAia_8J4IGM1t1GwnpwY_ZW7LtQ2LyorzHLX8GL3hFf3g130_assertion description "[The valine variant of MnSOD signal peptide increases the risk of VSA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92167.RAia_8J4IGM1t1GwnpwY_ZW7LtQ2LyorzHLX8GL3hFf3g130_provenance.
- NP92169.RAiiy9JTa2t6rK3_Vaq9Y43gUld6hCxT7byJuskJBwtsE130_assertion description "[The CTD could effectively relieve the symptoms of TD, its efficacy might be related with the genotype of SOD, and 9Ala is considered to be a protective factor for the susceptibility to TD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92169.RAiiy9JTa2t6rK3_Vaq9Y43gUld6hCxT7byJuskJBwtsE130_provenance.
- NP92171.RAh4HUw4FgkqnNpgWpgb9uL8GHWcFAnE91dSpt4rVTiX8130_assertion description "[Analysis of two polymorphisms of the manganese superoxide dismutase gene (Ile-58Thr and Ala-9Val) in patients with recurrent depressive disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92171.RAh4HUw4FgkqnNpgWpgb9uL8GHWcFAnE91dSpt4rVTiX8130_provenance.
- NP92176.RAkP1VRJ7td7PAJDeNCdL3KPMEGDQyrZoG2H8icK9ow5w130_assertion description "[Common polymorphisms in ITGA2, PON1 and THBS2 are associated with coronary atherosclerosis in a candidate gene association study of the Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92176.RAkP1VRJ7td7PAJDeNCdL3KPMEGDQyrZoG2H8icK9ow5w130_provenance.
- NP92181.RAjpRWEIbx3cir3O3P4t4Mv_doVLWqWpMjsNBIxDhDUnI130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92181.RAjpRWEIbx3cir3O3P4t4Mv_doVLWqWpMjsNBIxDhDUnI130_provenance.
- NP92182.RAhsB7UgXfGPMGuAQ6pSXDY0DbHHY0caZvNEvsQ0htELY130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92182.RAhsB7UgXfGPMGuAQ6pSXDY0DbHHY0caZvNEvsQ0htELY130_provenance.
- NP92184.RAkpBPzuXygEiohVrBr7dwgOokTgDhD9apYKmeN0CmRYI130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92184.RAkpBPzuXygEiohVrBr7dwgOokTgDhD9apYKmeN0CmRYI130_provenance.
- NP92186.RAh0SjuUi0cUYzyNRylV7cBkSIUeRNb_kt6NSMq23G4GU130_assertion description "[Support Vector Machine based feature selection method in this research found novel association between combinations of SNPs and T2D in a Korean population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92186.RAh0SjuUi0cUYzyNRylV7cBkSIUeRNb_kt6NSMq23G4GU130_provenance.
- NP92189.RArkBnJkVDXxQWJr6kwZdL_1hCmEI0xhcGIYo7OKLqYoo130_assertion description "[The association between survivor motor neuron (SMN) gene deletions and motor neuron diseases such as spinal muscular atrophy (SMA) and amyotrophic lateral sclerosis (ALS) suggest that sporadic lower motor neuron disease (LMND) may be related to SMN gene deletion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92189.RArkBnJkVDXxQWJr6kwZdL_1hCmEI0xhcGIYo7OKLqYoo130_provenance.
- NP92192.RAt2HSvrSP5OYTHQ3r7ZaatmRf1bo-rJtUr0sJhi3l7iM130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92192.RAt2HSvrSP5OYTHQ3r7ZaatmRf1bo-rJtUr0sJhi3l7iM130_provenance.
- NP92193.RApRkeAOrMBcJ2RolMaMrOykr8QrZlYezBKLyg146DaU8130_assertion description "[Polymorphisms at LDLR locus may be associated with coronary artery disease through modulation of coagulation factor VIII activity and independently from lipid profile.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92193.RApRkeAOrMBcJ2RolMaMrOykr8QrZlYezBKLyg146DaU8130_provenance.
- NP92195.RAkV1NnIKyOm91L6gp-u_hFlLb7mtGLRudfizNhq3C8lQ130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92195.RAkV1NnIKyOm91L6gp-u_hFlLb7mtGLRudfizNhq3C8lQ130_provenance.
- NP92198.RAgqC7aEB6fc19DJIk35127XgJWRmv4toDnNP0ZeBq14E130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92198.RAgqC7aEB6fc19DJIk35127XgJWRmv4toDnNP0ZeBq14E130_provenance.
- NP92200.RAqgsie5bmvXMMOPFWeAfbnTtiyoZK7-J38JtawKS7cuc130_assertion description "[SNPs and haplotypes in SLC9A3 in whites and SLC4A1 and SLCO4C1 in blacks are significantly associated with preeclampsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92200.RAqgsie5bmvXMMOPFWeAfbnTtiyoZK7-J38JtawKS7cuc130_provenance.
- NP92203.RAvmGBP1AJ0m_HT32oDDnUXBxpsILfipIxtl3Sk4jV91Q130_assertion description "[We targeted CNRs of cardiovascular disease (CVD) candidate gene, Na(+)-Ca(2+) exchanger (NCX1) with polymorphism screening among CVD patients (n = 46) using DHPLC technology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92203.RAvmGBP1AJ0m_HT32oDDnUXBxpsILfipIxtl3Sk4jV91Q130_provenance.
- NP92206.RAriE_TYPWLJUUK9G64UWKuXLUKicPGrQVhbXXc8jW8R4130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92206.RAriE_TYPWLJUUK9G64UWKuXLUKicPGrQVhbXXc8jW8R4130_provenance.
- NP92207.RApmXf-yS-GewQffQKWnlfW7neyv1K_dfj4kXmy6H8AZ0130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92207.RApmXf-yS-GewQffQKWnlfW7neyv1K_dfj4kXmy6H8AZ0130_provenance.
- NP92208.RAlt3UV52oe0ujYV4vp6NBBRLzsb7dg20959D1wGXIw10130_assertion description "[These results suggest that CACNA1C may be associated with secondary hyperparathyroidism. In addition, the haplotype-based approach may be useful to screen for key molecules associated with complex traits.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92208.RAlt3UV52oe0ujYV4vp6NBBRLzsb7dg20959D1wGXIw10130_provenance.
- NP92209.RAj4R-jyoRwMhfKigltTtvQPJNgLN-mjI6x32J2rv7ym0130_assertion description "[A new association between polymorphisms of the SLC6A7 gene in the chromosome 5q31-32 region and asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92209.RAj4R-jyoRwMhfKigltTtvQPJNgLN-mjI6x32J2rv7ym0130_provenance.