Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP53216.RAvuWFHKLp8nCQOh8y-YitgAXqeuHHv-hgg0F9HXkOVzc130_assertion description "[Association of progesterone receptor polymorphisms with recurrent implantation failure after in vitro fertilization and embryo transfer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53216.RAvuWFHKLp8nCQOh8y-YitgAXqeuHHv-hgg0F9HXkOVzc130_provenance.
- NP53228.RAiWiQoklLD58APxNGI9aWzSqCZ85HbLtwxmTH5tFjAYo130_assertion description "[ Our results suggest that the IVS2 + 11A/C allele may be involved in the development of asthma in the Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53228.RAiWiQoklLD58APxNGI9aWzSqCZ85HbLtwxmTH5tFjAYo130_provenance.
- NP53229.RAr3mYPpK3IODD_PZ4mNDQKu_crfp-FCGnEcsBJ7pm4Io130_assertion description "[Nonsense mutation in the phosphofructokinase muscle subunit gene associated with retention of intron 10 in one of the isolated transcripts in Ashkenazi Jewish patients with Tarui disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53229.RAr3mYPpK3IODD_PZ4mNDQKu_crfp-FCGnEcsBJ7pm4Io130_provenance.
- NP53233.RAskYd0GEHsPGJRXf78PTc9e20OcvF-JqZ4agCVpVE3s8130_assertion description "[ These data suggest that the ICAM-1 469KK genotype could be a genetic risk factor for retinopathy in Type 2 diabetes mellitus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53233.RAskYd0GEHsPGJRXf78PTc9e20OcvF-JqZ4agCVpVE3s8130_provenance.
- NP53238.RAir4_XGgpKTcM3QuTewsvBk5esRLDZSfJrCyRytpmMoQ130_assertion description "[Role of non-HLA genetic polymorphisms in graft-versus-host disease after haematopoietic stem cell transplantation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53238.RAir4_XGgpKTcM3QuTewsvBk5esRLDZSfJrCyRytpmMoQ130_provenance.
- NP53241.RAs3kolX9Ua384mkRGB-_jEiaz1Cr8xidgq4VXUDJYLbc130_assertion description "[We hypothesized that genetic variation and the level of soluble PECAM-1 could be associated with the development of atherosclerosis and conducted a study on gene polymorphisms of PECAM-1 and soluble PECAM-1 levels in Asian Indian patients with coronary artery disease (CAD) in Singapore.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53241.RAs3kolX9Ua384mkRGB-_jEiaz1Cr8xidgq4VXUDJYLbc130_provenance.
- NP53253.RApFkvykYDPvL-jpBluiNuZrWf2rFlFoX27_UmE7eAu2Q130_assertion description "[These results suggest that PDLIM5 might play a role in genetic susceptibility to schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53253.RApFkvykYDPvL-jpBluiNuZrWf2rFlFoX27_UmE7eAu2Q130_provenance.
- NP53254.RAo5wyqtUsLFapwZtE6AUzXAuNx6uUSX7WBY42yKqPvgk130_assertion description "[Further, we failed to find any genetic association between the PDLIM5 gene and schizophrenia with six single nucleotide polymorphics (SNPs) of the PDLIM5 gene in Japanese subjects (279 subjects each) and there was no significant relation between PDLIM5 gene and schizophrenia with the haplotype analysis (P=0.48), either.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53254.RAo5wyqtUsLFapwZtE6AUzXAuNx6uUSX7WBY42yKqPvgk130_provenance.
- NP53257.RAp7TI-KyW3bBvXukkoQ6MDHRE8stlvuhLjdSNASc3VyE130_assertion description "[ The results of these preliminary analyses suggest that genetic anomalies of the TGFbeta1 and PDGF gene families are not likely to explain the dysregulation seen in SSc or to account for the susceptibility to SSc in this population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53257.RAp7TI-KyW3bBvXukkoQ6MDHRE8stlvuhLjdSNASc3VyE130_provenance.
- NP53262.RAi2bJbfg4JrC1FtH0UPjrqjLFU1J5mcv1hZPjE_GYUbk130_assertion description "[Conditional logistic regression calculations revealed no significant association of ischemic stroke to the defined at-risk allele in PDE4D (odds ratio, 1.1; 95% confidence interval, 0.84 to 1.45).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53262.RAi2bJbfg4JrC1FtH0UPjrqjLFU1J5mcv1hZPjE_GYUbk130_provenance.
- NP53264.RAsM9n_aZpwS8FCF4IJpmMunr-83TAQ1CEFJePxDaOtCM130_assertion description "[In this study, we aimed at investigating the association between 3 polymorphisms of the PDE4D gene and ischemic stroke in the Pakistani population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53264.RAsM9n_aZpwS8FCF4IJpmMunr-83TAQ1CEFJePxDaOtCM130_provenance.
- NP53272.RAkcfQ_7lzCbH5DnJzt0e0piY2bGUAwhYn9PGcrT_LqKI130_assertion description "[In this study, we performed a genetic association study on the single nucleotide polymorphisms (SNPs) present in the genes CD14 (-159 C/T), TNFalpha (-308 G/A), IL-1alpha (-889 C/T), IL-6 (-174 G/C), PSMA6 (-8 C/G), and PDE4D (SNP83 T/C, respectively) in order to discern their possible role in the susceptibility to stroke in a North Indian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53272.RAkcfQ_7lzCbH5DnJzt0e0piY2bGUAwhYn9PGcrT_LqKI130_provenance.
- NP53273.RAlckU1C53jq90o2EXDgOtTvVNHs0nVOq2lZd4Lz_0VyI130_assertion description "[Thus, the identified polymorphisms are unlikely to have major effects on susceptibility to Japanese type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53273.RAlckU1C53jq90o2EXDgOtTvVNHs0nVOq2lZd4Lz_0VyI130_provenance.
- NP53277.RAmQYOWviU-h5R_NOz_-RqjJo5zTIJ3mzjRgGK_3uix3U130_assertion description "[Here, we analyzed 2,510 individuals, including members of five independent sets of families as well as unrelated individuals affected with SLE, for single-nucleotide polymorphisms (SNPs) that we identified in PDCD1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53277.RAmQYOWviU-h5R_NOz_-RqjJo5zTIJ3mzjRgGK_3uix3U130_provenance.
- NP53279.RAvfrakkR88PuIbXG7IKNQDKVWz48EFp4gErygHmAQe04130_assertion description "[We evaluated the roles of five single-nucleotide polymorphisms (SNPs) within PDCD1, and haplotypes defined by these SNPs, for the development of systemic lupus erythematosus (SLE) and specific sub-phenotypes (nephritis, antiphospholipid antibody positive, arthritis and double-stranded DNA positive) within a multiethnic US cohort of 1036 patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53279.RAvfrakkR88PuIbXG7IKNQDKVWz48EFp4gErygHmAQe04130_provenance.
- NP53280.RAvH7GemBfDp4474yoggu_4i73y6qZoT7KVaivh4h6KlI130_assertion description "[To investigate the role of programmed cell death-1 (PD-1) gene polymorphisms in the development of systemic lupus erythematosus (SLE) in Taiwan, 109 patients with SLE and 100 healthy controls were enrolled in this study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53280.RAvH7GemBfDp4474yoggu_4i73y6qZoT7KVaivh4h6KlI130_provenance.
- NP53288.RAt3Rb56FWLnbK8mBdJpyoP5L56v_Gx72mwF6cDfubMtk130_assertion description "[A regulatory polymorphism in PDCD1 is associated with susceptibility to systemic lupus erythematosus in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53288.RAt3Rb56FWLnbK8mBdJpyoP5L56v_Gx72mwF6cDfubMtk130_provenance.
- NP53291.RAjQErgUsTueGFpOvuJWgNHJ4nzTKss6TbH5FufXIilpw130_assertion description "[Association between the PD1.3A/G polymorphism of the PDCD1 gene and systemic lupus erythematosus in European populations: a meta-analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53291.RAjQErgUsTueGFpOvuJWgNHJ4nzTKss6TbH5FufXIilpw130_provenance.
- NP53293.RArUwcNKJeFZdlJcy-46_ThOmXwOE9ZeBaqUG2Zq49NoA130_assertion description "[were stratified by reanalyzing genotype data with relevant symptoms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53293.RArUwcNKJeFZdlJcy-46_ThOmXwOE9ZeBaqUG2Zq49NoA130_provenance.
- NP53295.RAnhc5lrjplkI6UkUxi0tYDkmtDAqm4jc6pNELLFZ3A1c130_assertion description "[Genetic screening protocol for familial hypercholesterolemia which includes splicing defects gives an improved mutation detection rate.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53295.RAnhc5lrjplkI6UkUxi0tYDkmtDAqm4jc6pNELLFZ3A1c130_provenance.
- NP53302.RAodlGPKr894fTVLC9TJt8jRl4v2Yz9BVrXsNoxJjlzcs130_assertion description "[Here, we analyzed 2,510 individuals, including members of five independent sets of families as well as unrelated individuals affected with SLE, for single-nucleotide polymorphisms (SNPs) that we identified in PDCD1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53302.RAodlGPKr894fTVLC9TJt8jRl4v2Yz9BVrXsNoxJjlzcs130_provenance.
- NP53305.RAuNqQyXhLuHNBXG5JBKPbe-Jf35ou4d1e-yUMTSxTO-Y130_assertion description "[Our study did not reveal an association between the PC-1 amino acid variant K121Q and progression of diabetic nephropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53305.RAuNqQyXhLuHNBXG5JBKPbe-Jf35ou4d1e-yUMTSxTO-Y130_provenance.
- NP53308.RAs_sTLJ3B1o8ri6QBWvIwK3h74xwl1I0O-d5tddpMbF8130_assertion description "[Adding SNPs previously associated with fasting glucose, insulin, lipids or obesity to a genetic risk score for type 2 diabetes significantly increases the power to discriminate between people with and without clinically manifest type 2 diabetes compared with a model including only conventional type 2 diabetes loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53308.RAs_sTLJ3B1o8ri6QBWvIwK3h74xwl1I0O-d5tddpMbF8130_provenance.
- NP53311.RAnzp16t_l31Hkm3cNh9h47hSbyGxZ5I7lJ37G-vWvy_M130_assertion description "[Association of the proprotein convertase subtilisin/kexin-type 2 (PCSK2) gene with type 2 diabetes in an African American population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53311.RAnzp16t_l31Hkm3cNh9h47hSbyGxZ5I7lJ37G-vWvy_M130_provenance.
- NP53316.RAmgccAFjjKvLDK5oKVPtBQdUM2AeZYs2ix3G8DS1n6lg130_assertion description "[Common PCSK1 haplotypes are associated with obesity in the Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53316.RAmgccAFjjKvLDK5oKVPtBQdUM2AeZYs2ix3G8DS1n6lg130_provenance.
- NP53317.RAr_3xCDoV4KbETt2ND_b1K0KJBGoxx0YKp-nBVpG9CSw130_assertion description "[Obesity-related polymorphisms and their associations with the ability to regulate fat oxidation in obese Europeans: the NUGENOB study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53317.RAr_3xCDoV4KbETt2ND_b1K0KJBGoxx0YKp-nBVpG9CSw130_provenance.
- NP53322.RAja81UvpN7yte-Yi1fKR1I7wDmbjqH0tquKnpJjJXfLc130_assertion description "[Polymorphisms of DNA repair genes and risk of non-small cell lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53322.RAja81UvpN7yte-Yi1fKR1I7wDmbjqH0tquKnpJjJXfLc130_provenance.
- NP53325.RAougK6fdJdHCuSkizk5HAjRHf4KnXbXlpfi5tXCsgn4U130_assertion description "[Thus, we report a promoter SNP in PCK1 that was resistant to down-regulation by insulin in vitro and was associated with type 2 DM in two independent study samples.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53325.RAougK6fdJdHCuSkizk5HAjRHf4KnXbXlpfi5tXCsgn4U130_provenance.
- NP53327.RApOMD6lnq-F8inGlldBq9Rk30oE8sXaxlxyV9jvAlDZA130_assertion description "[The PCK1 gene, encoding cytosolic phosphoenolpyruvate carboxykinase (PEPCK-C), has previously been implicated as a candidate gene for type 2 diabetes (T2D) susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53327.RApOMD6lnq-F8inGlldBq9Rk30oE8sXaxlxyV9jvAlDZA130_provenance.
- NP53332.RAs4VA8zoJsad_imO8Vys2AuRD3jqbS6oRWPrCFMhDME4130_assertion description "[In a case-control study of 655 unrelated individuals, allele frequencies and genotype distributions of the functional PAX-6 promoter polymorphism were investigated comprising patients with DSM-IV schizophrenia, patients with affective disorders, and population controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53332.RAs4VA8zoJsad_imO8Vys2AuRD3jqbS6oRWPrCFMhDME4130_provenance.
- NP53333.RAqHWRiqVsMp7uBq58_xSvpR2cilYZSB8_smd9t13fQl8130_assertion description "[We found negative correlation between numbers of PAX-6 gene promoter B (AC)m (AG)n repeats and atrophy of the brain and the cerebellum. Occurrence of these lesions was correlated with a decrease of alcohol tolerance, withdrawal symptoms--especially delirium tremens.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53333.RAqHWRiqVsMp7uBq58_xSvpR2cilYZSB8_smd9t13fQl8130_provenance.
- NP53334.RAnZubuJ1lVxrbLeFzg70qvoJZOc15_zATK431_OloUFw130_assertion description "[This is the first report of a Pax4 gene mutation that exhibits loss of function and seems to be associated with type 2 diabetes. This work provides significant implications for the Pax4 gene as one of the predisposing genes for type 2 diabetes in the Japanese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53334.RAnZubuJ1lVxrbLeFzg70qvoJZOc15_zATK431_OloUFw130_provenance.
- NP53354.RAtOLxSI8nXKgIhz30hQuV981etBp_av6H-HrwwB6FhEg130_assertion description "[Do polymorphisms in the familial Parkinsonism genes contribute to risk for sporadic Parkinson's disease?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53354.RAtOLxSI8nXKgIhz30hQuV981etBp_av6H-HrwwB6FhEg130_provenance.
- NP53358.RAq2HGQasev-6K3v3z_UMp1p_YFgrzemBsld5uGN-DlLg130_assertion description "[Association study of major risk single nucleotide polymorphisms in the common regulatory region of PARK2 and PACRG genes with leprosy in an Indian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53358.RAq2HGQasev-6K3v3z_UMp1p_YFgrzemBsld5uGN-DlLg130_provenance.
- NP53367.RAt9h_-7XNgo1k8jwHBHYrFQfaeCyfOlzCKCAQY--jxSE130_assertion description "[Analysis of Parkinson disease patients from Portugal for mutations in SNCA, PRKN, PINK1 and LRRK2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53367.RAt9h_-7XNgo1k8jwHBHYrFQfaeCyfOlzCKCAQY--jxSE130_provenance.
- NP53385.RAmyRZZVqlKw_2FhClzen5NeVCix1E_xEbfG_mF44QVBY130_assertion description "[The Ile198Thr and Ala379Val variants of plasmatic PAF-acetylhydrolase impair catalytical activities and are associated with atopy and asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53385.RAmyRZZVqlKw_2FhClzen5NeVCix1E_xEbfG_mF44QVBY130_provenance.
- NP53386.RAs9pAvVKfCu4LMRW4hW7v5W68jd7rjEgTtC42a7XtfX4130_assertion description "[Association of a G994 --> T (Val279 --> Phe) polymorphism of the plasma platelet-activating factor acetylhydrolase gene with myocardial damage in Japanese patients with nonfamilial hypertrophic cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53386.RAs9pAvVKfCu4LMRW4hW7v5W68jd7rjEgTtC42a7XtfX4130_provenance.
- NP53390.RAgPNI1sFlDZPj_QWdhPO8dGJe28WWxg-x-i1rhloLa10130_assertion description "[Polymorphisms and haplotypes of the peptidylarginine deiminase type 4 gene (PADI4) have been reported to be associated with rheumatoid arthritis (RA) in a Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53390.RAgPNI1sFlDZPj_QWdhPO8dGJe28WWxg-x-i1rhloLa10130_provenance.
- NP53399.RAn37jkQxKc4FOJdW_QRlwLK2rxdI8da7IsGbgQoEgwaE130_assertion description "[Twenty-three polymorphisms in 22 potential PAD candidate genes (F2, FGB, MTHFR, ITGB3, ACE, AGT, IL6, CCL2, ICAM1, SELE, MMP9, PPARG, MMP1, ADD1, P2RY12, LIPC, PLA2G7, SCARB1, MMP3, MTTP, LPA, CHRNA3) showed a significant association in individual studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53399.RAn37jkQxKc4FOJdW_QRlwLK2rxdI8da7IsGbgQoEgwaE130_provenance.
- NP53407.RAlIyFmn1_PPnbg0d7GG8RlIe31llo2XJJp2dqum3OQrs130_assertion description "[The P2X7 receptor, a plasma membrane ATP-gated ion channel that plays a role in lymphocyte apoptosis, has been suggested as an important contributory factor to the pathogenesis of chronic lymphocytic leukaemia (CLL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53407.RAlIyFmn1_PPnbg0d7GG8RlIe31llo2XJJp2dqum3OQrs130_provenance.
- NP53409.RAi9-_qEESvwFUKQX-h1f3lpph2_UXEz-fatDw3va9TwY130_assertion description "[The results obtained in this study argue against associations of specific single nucleotide polymorphisms in the PALLD, ROS1, TAS2R50, OR13G1, and ZNF627 genes with myocardial infarction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53409.RAi9-_qEESvwFUKQX-h1f3lpph2_UXEz-fatDw3va9TwY130_provenance.
- NP53412.RArufWkuJg-qmtOKoIAAHb4C9fkgbJozuEzfVxdKlPV-M130_assertion description "[Genes related to sex steroids, neural growth, and social-emotional behavior are associated with autistic traits, empathy, and Asperger syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53412.RArufWkuJg-qmtOKoIAAHb4C9fkgbJozuEzfVxdKlPV-M130_provenance.
- NP53416.RAqhFolcU1aqlxGmG9YPWLvk3HA3KgZK3OXtQ7o0_MhVc130_assertion description "[Association of the oxytocin receptor (OXTR) gene polymorphisms with autism spectrum disorder (ASD) in the Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53416.RAqhFolcU1aqlxGmG9YPWLvk3HA3KgZK3OXtQ7o0_MhVc130_provenance.
- NP53418.RAt8JcLWQQavAl1iBy6NThlK1Y301TNyoocU_m6joMCYk130_assertion description "[Genes controlling affiliative behavior as candidate genes for autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53418.RAt8JcLWQQavAl1iBy6NThlK1Y301TNyoocU_m6joMCYk130_provenance.
- NP53437.RAjl-mVT_LGdVWLOjLXsBCEa2R6o-l2splPYTH_xTe0po130_assertion description "[The purpose of this study was to investigate associations between 13 single nucleotide polymorphisms in the mu opioid receptor gene (OPRM1) with self-reported responses to alcohol, an endophenotype associated with the development of alcohol dependence, in American Indians living on eight contiguous reservations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53437.RAjl-mVT_LGdVWLOjLXsBCEa2R6o-l2splPYTH_xTe0po130_provenance.
- NP53445.RAl-F_s1JbEb5PVaHg5dxvlogCE_TaBUdCeCJL0y3TPY0130_assertion description "[ These findings fail to support the hypothesis that Asn40Asp alleles moderate the development of personality dimensions, as measured by the Five-Factor Model.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53445.RAl-F_s1JbEb5PVaHg5dxvlogCE_TaBUdCeCJL0y3TPY0130_provenance.
- NP53447.RAvlc1x6sUklFWrhBkzSX6V8zfSmow4MMUxc5sn0zBP6E130_assertion description "[This study suggests that the variant G allele of both A118G and C1031G polymorphisms may contribute to the vulnerability to heroin dependence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53447.RAvlc1x6sUklFWrhBkzSX6V8zfSmow4MMUxc5sn0zBP6E130_provenance.
- NP53449.RAhfoiu2IC-0t39I0qPlbJ5w_kdUCsezTGT3_kFEPyqJ4130_assertion description "[These results suggest that DRD2 genotype may contribute to the understanding of the interindividual variability to the response to MMT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53449.RAhfoiu2IC-0t39I0qPlbJ5w_kdUCsezTGT3_kFEPyqJ4130_provenance.
- NP53451.RApAdzB-ITWo0xD3gho5aXRawSS8ovS1NXUpKZ0SZhWac130_assertion description "[These results confirm the previous association and support the hypothesis of a role for OPRM1 in IGE, including absence syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53451.RApAdzB-ITWo0xD3gho5aXRawSS8ovS1NXUpKZ0SZhWac130_provenance.
- NP53454.RApfBuy3zC3N28d3NDaPROqAh88AjoM1hKRMiKoWQBrwc130_assertion description "[Sequence variability and candidate gene analysis in complex disease: association of mu opioid receptor gene variation with substance dependence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53454.RApfBuy3zC3N28d3NDaPROqAh88AjoM1hKRMiKoWQBrwc130_provenance.
- NP53456.RArlQR-keB4iyOWlpEpjXxf6NWX3TxqSgf5WJ-InZOhDo130_assertion description "[ These findings may help to explain previous research suggesting that naltrexone is more effective among individuals with the G allele. A medication that reduces feelings of euphoria after alcohol consumption may be more successful among individuals with a genetic predisposition to greater feelings of euphoria after consuming alcohol.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53456.RArlQR-keB4iyOWlpEpjXxf6NWX3TxqSgf5WJ-InZOhDo130_provenance.
- NP53457.RArFRm3JyeP2jsgXSeIzav7YK2BqoYiBDsj-I8Ak5BzEE130_assertion description "[In central Sweden, the functional variant 118G allele in exon 1 of OPRM1 is associated with an increased attributable risk for alcohol dependence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53457.RArFRm3JyeP2jsgXSeIzav7YK2BqoYiBDsj-I8Ak5BzEE130_provenance.
- NP53459.RAqhXQtrhn3t_cpl-d_dLnfIsQLwL07sWT_oIYvKTn3SE130_assertion description "[The contribution of the gene to risk for substance dependence is small, and is detected most easily in studies that use control samples that are screened for all forms of substance dependence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53459.RAqhXQtrhn3t_cpl-d_dLnfIsQLwL07sWT_oIYvKTn3SE130_provenance.
- NP53466.RAnASmaEhr_X8j77xZUgNRPZnXHKvoUjQRbNPPcqfzrLw130_assertion description "[Using logistic regression with opioid dependence as the dependent variable, the 36G>T SNP exhibited a point-wise significant association (P = 0.016) with disease status. The number of haplotypes seen in the three ethnic groups were nine, six and five for African-Americans, Caucasians, and Hispanics, respectively, with corresponding significance levels for differences in haplotype frequencies between cases and controls of P = 0.0742, 0.1015 and 0.0041. Combining ethnicities by Fisher's method yields an empirical significance level of P = 0.0020.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53466.RAnASmaEhr_X8j77xZUgNRPZnXHKvoUjQRbNPPcqfzrLw130_provenance.
- NP53468.RAs5DWs7Srng61hAmFee33QLi4Zd5EhPpMTRzc11jnahI130_assertion description "[Human tritanopia associated with two amino acid substitutions in the blue-sensitive opsin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53468.RAs5DWs7Srng61hAmFee33QLi4Zd5EhPpMTRzc11jnahI130_provenance.
- NP53471.RAvGU2iOedHhJhkq_pQoysdeaYcKcjJpfjcUbcEuG374A130_assertion description "[Investigating the association between OPA1 polymorphisms and glaucoma: comparison between normal tension and high tension primary open angle glaucoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53471.RAvGU2iOedHhJhkq_pQoysdeaYcKcjJpfjcUbcEuG374A130_provenance.
- NP53472.RAtGoCuw082s3-cBx1Fo9qEtjPBe8pQGo5FvTuqrlNFQo130_assertion description "[To assess whether genetic polymorphisms of optic atrophy 1 (OPA1) are associated with primary open-angle glaucoma (POAG).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53472.RAtGoCuw082s3-cBx1Fo9qEtjPBe8pQGo5FvTuqrlNFQo130_provenance.
- NP53475.RAvgNOhVbVNH1o5WtOuUTNnVIYBUuohi5tL5_06OrsQVk130_assertion description "[We have refined the previously reported association between OPA1 sequence changes and NTG by identifying a specific CC genotype at position +32 in IVS8 of the OPA1 gene that acts as a marker for NTG.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53475.RAvgNOhVbVNH1o5WtOuUTNnVIYBUuohi5tL5_06OrsQVk130_provenance.
- NP53479.RAp5wav5Z2qRyoXQcvmJ9hWZpNQ-A4qExS842JUg33YZ0130_assertion description "[Our data suggest that genetic variation in the OLR1 gene may modify the risk of AD in an APOE*4-dependent fashion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53479.RAp5wav5Z2qRyoXQcvmJ9hWZpNQ-A4qExS842JUg33YZ0130_provenance.
- NP53480.RAu9S9TXD_twOnEFIeZQHzm1HEgepPQFa2HtSlZSlXLag130_assertion description "[The OLR1 expression was significantly lower in AD cases bearing the CC and CT genotypes compared with controls with the same genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53480.RAu9S9TXD_twOnEFIeZQHzm1HEgepPQFa2HtSlZSlXLag130_provenance.
- NP53483.RAoTee02wUk6Tkc6ItIEG4Shf3YMgjdm-PCa9D6Nl5q0U130_assertion description "[Alpha-2-macroglobulin gene, oxidized low-density lipoprotein receptor-1 locus, and sporadic Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53483.RAoTee02wUk6Tkc6ItIEG4Shf3YMgjdm-PCa9D6Nl5q0U130_provenance.
- NP53487.RAvVWUe_2XfIhym2ZKWVPFiMFzsZgyq8uE0k80u0IC_s0130_assertion description "[The overall effects of these genetic polymorphisms were moderate in terms of relative risk, with ORs ranging from 2-10. There was also some evidence that genetic polymorphisms in certain carcinogen-metabolizing enzymes such as CYP2E1, CYP1A1, CYP2A6, GSTM1, and GSTP1 modulate risk of the cancer, although the results require confirmation with larger]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53487.RAvVWUe_2XfIhym2ZKWVPFiMFzsZgyq8uE0k80u0IC_s0130_provenance.
- NP53489.RAhDLbkag6FOpB9Etv8YRBkPqgXQ4IixSmzKVthfeqNwY130_assertion description "[We conducted a case-control study to investigate the association between OGG1 Ser326Cys polymorphism and the risk of lung cancer using PCR-RFLP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53489.RAhDLbkag6FOpB9Etv8YRBkPqgXQ4IixSmzKVthfeqNwY130_provenance.
- NP53492.RAudmTF-MF8OH1uuUZjwHqcJJZtYmVD27_E33AwGhlX_4130_assertion description "[Interactions between the OGG1 Ser326Cys polymorphism and intake of fruit and vegetables in relation to lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53492.RAudmTF-MF8OH1uuUZjwHqcJJZtYmVD27_E33AwGhlX_4130_provenance.
- NP53493.RAhYQco4s7CcNircmaO3c98HMtNOVJxQwSev-uFYA45wA130_assertion description "[Our results indicate that SNPs in the NER genes ERCC1 (Asn118Asn, 15310G>C, 8902G>T), XPA (-4G>A), ERCC2/XPD (Lys751Gln) and ERCC5/XPD (His46His); the BER genes APE1/APEX (Ile64Val), OGG1 (Ser326Cys), PCNA (1876A>G) and XRCC1 (Arg194Trp, Arg280His, Arg399Gln); and the DSB-R genes ATR (Thr211Met), NBS1 (Glu185Gln), XRCC2 (Arg188His) and XRCC9 (Thr297Ile) modulate NSCLC risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53493.RAhYQco4s7CcNircmaO3c98HMtNOVJxQwSev-uFYA45wA130_provenance.
- NP53502.RAh-rME3joXeGGB4w3-GEoVmp7DK5XutE8d_OS921UFBo130_assertion description "[Common polymorphisms in the XPD and hOGG1 genes are not associated with the risk of colorectal cancer in a Polish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53502.RAh-rME3joXeGGB4w3-GEoVmp7DK5XutE8d_OS921UFBo130_provenance.
- NP53503.RApsz0bZO_bCcrcWE1Z8O19avOAHTLCUq7vhkI494kqpQ130_assertion description "[GPX1 Pro(198)Leu polymorphism, erythrocyte GPX activity, interaction with alcohol consumption and smoking, and risk of colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53503.RApsz0bZO_bCcrcWE1Z8O19avOAHTLCUq7vhkI494kqpQ130_provenance.
- NP53506.RAnY8EnUhsTJATOHNjidQoTjAsP1gQnY3DPR7snYjvFqc130_assertion description "[DNA repair single-nucleotide polymorphisms in colorectal cancer and their role as modifiers of the effect of cigarette smoking and alcohol in the Singapore Chinese Health Study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53506.RAnY8EnUhsTJATOHNjidQoTjAsP1gQnY3DPR7snYjvFqc130_provenance.
- NP53507.RAggaDxg2ZLfHYFyZY4ujzXti4Ozn5-rPtoZvvssVvHB0130_assertion description "[DNA repair genetic polymorphisms and risk of colorectal cancer in the Czech Republic.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53507.RAggaDxg2ZLfHYFyZY4ujzXti4Ozn5-rPtoZvvssVvHB0130_provenance.
- NP53510.RAleSISX0RS1RP32q855-h0nQAq_8zNA45akw6XHjBPeU130_assertion description "[We undertook a case-control study of 212 urothelial bladder cancer (UBC) cases and 250 controls to investigate the association between OGG1 (C1245G rs1052133), XRCC3 (C18067T, rs861539) and XRCC7 (G6721T, rs7003908) polymorphisms and bladder cancer susceptibility by PCR-RFLP and the ARMS method.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53510.RAleSISX0RS1RP32q855-h0nQAq_8zNA45akw6XHjBPeU130_provenance.
- NP53511.RAqDhhRwyqs7wys1UWlOdp7_BdTwnD5e7HAe7L66ElkN4130_assertion description "[In order to examine the association of common genetic variation in the base-excision repair (BER) pathway with bladder cancer risk, we analyzed 43 single nucleotide polymorphisms (SNPs) in 12 BER genes (OGG1, MUTYH, APEX1, PARP1, PARP3, PARP4, XRCC1, POLB, POLD1, PCNA, LIG1, and LIG3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53511.RAqDhhRwyqs7wys1UWlOdp7_BdTwnD5e7HAe7L66ElkN4130_provenance.
- NP53518.RAvxHqEAQ-RhlJSnjamWdPDgV9cz37SobHYWmj2h8jCj8130_assertion description "[hOGG1 Ser326Cys polymorphism and susceptibility to gallbladder cancer in a Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53518.RAvxHqEAQ-RhlJSnjamWdPDgV9cz37SobHYWmj2h8jCj8130_provenance.
- NP53525.RAlDKjmeFwlG5CWjczpEfo2hHaANAbq6bxm_yuCeSgpWg130_assertion description "[Pooled data from two population-based studies (1,457 cases and 1,351 controls) were analyzed to examine associations between 28 single-nucleotide polymorphisms (SNPs) in nine DNA repair genes (APEX1, BRCA2, ERCC2, ERCC4, MGMT, MUTYH, OGG1, XPC, and XRCC1) and prostate cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53525.RAlDKjmeFwlG5CWjczpEfo2hHaANAbq6bxm_yuCeSgpWg130_provenance.
- NP53532.RAssxtsn365n0GtkRQ1kiGO5PkrQFGcVs7CV751nystiE130_assertion description "[By comparing allelic distribution between cases and controls, we show that MM and OCA2 are associated (p value=0.030 after correction for multiple testing).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53532.RAssxtsn365n0GtkRQ1kiGO5PkrQFGcVs7CV751nystiE130_provenance.
- NP53533.RAhFf4TG-9VjMEJy-Re0JKtWzWbD_YvIdHOnVl7R7dgdw130_assertion description "[SLC45A2: a novel malignant melanoma-associated gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53533.RAhFf4TG-9VjMEJy-Re0JKtWzWbD_YvIdHOnVl7R7dgdw130_provenance.
- NP53545.RAkYmClRrP62o1UyL4zuJTlQyAdTgRkVGJ0bKED2hkuNs130_assertion description "[Polymorphisms of interferon-inducible genes OAS-1 and MxA associated with SARS in the Vietnamese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53545.RAkYmClRrP62o1UyL4zuJTlQyAdTgRkVGJ0bKED2hkuNs130_provenance.
- NP53546.RAjgafvBXvCgkP0hkmvCjWxBHKtYwyvW9GdG0fLiiSvRk130_assertion description "[Association of SARS susceptibility with single nucleic acid polymorphisms of OAS1 and MxA genes: a case-control study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53546.RAjgafvBXvCgkP0hkmvCjWxBHKtYwyvW9GdG0fLiiSvRk130_provenance.
- NP53555.RAhlp4dQSN3dxcp_bwCy2KeiLRBbfZhElHZUWMDNFWEYU130_assertion description "[Association analysis of the proneurotensin gene and bipolar disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53555.RAhlp4dQSN3dxcp_bwCy2KeiLRBbfZhElHZUWMDNFWEYU130_provenance.
- NP53562.RArSDYm4AJFlCKweUO-1TFd5AmqLM4aFCBV9G3LRcW8h0130_assertion description "[The recent possible neurodevelopmental etiology of schizophrenia makes neurotrophin-3 (NT-3) gene an interesting candidate locus for molecular study of schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53562.RArSDYm4AJFlCKweUO-1TFd5AmqLM4aFCBV9G3LRcW8h0130_provenance.
- NP53565.RAuAATbFeoebUsVxcd2snIeZ0lm-66ylDSYz3qP68WQ7I130_assertion description "[Multilocus analyses of estrogen-related genes reveal involvement of the ESR1 gene in male infertility and the polygenic nature of the pathology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53565.RAuAATbFeoebUsVxcd2snIeZ0lm-66ylDSYz3qP68WQ7I130_provenance.
- NP53571.RAjyy9omcU1j3uRu9Si_FxMfyxTBQEcxfjVgJlHMapI8M130_assertion description "[We have previously reported an association between the T allele of the rs6994992 SNP within NRG1 gene and lateral ventricle (LV) enlargement in first-episode schizophrenia patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53571.RAjyy9omcU1j3uRu9Si_FxMfyxTBQEcxfjVgJlHMapI8M130_provenance.
- NP53574.RArQU42tJiJPIZ-XYravDXImBsQIeyeAkZQZi_WkUMdKQ130_assertion description "[Neuregulin-1 genotypes and eye movements in schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53574.RArQU42tJiJPIZ-XYravDXImBsQIeyeAkZQZi_WkUMdKQ130_provenance.
- NP53575.RAgcgQfvdodpTjoV6v_itIaLEyTht9Ds9tpBG6Smq4aoI130_assertion description "[While DTNBP1, DISC1, and NRG1 have been extensively studied as candidate genes of schizophrenia, results remain inconclusive.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53575.RAgcgQfvdodpTjoV6v_itIaLEyTht9Ds9tpBG6Smq4aoI130_provenance.
- NP53585.RAgHVB6YFqpW3R9jXGho8MshVW_Sq4aYa1L-qZkcl7nPk130_assertion description "[Family-based association study of Neuregulin 1 with psychotic bipolar disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53585.RAgHVB6YFqpW3R9jXGho8MshVW_Sq4aYa1L-qZkcl7nPk130_provenance.
- NP53588.RAs5MRHG4b86tybds061tlKy2zBNMTp9600y2-zeAGr1Q130_assertion description "[In conclusion, our data suggest that ras oncogene mutations might identify a group of leukaemia in people with previous X-ray/chemotherapy or with exposure to chemical agents in the work environment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53588.RAs5MRHG4b86tybds061tlKy2zBNMTp9600y2-zeAGr1Q130_provenance.
- NP53593.RAmoxDiNrjrOUEd51APtjnZPdMul0FX2KEmF4t26wAdyE130_assertion description "[Nuclear respiratory factor 1 (NRF1) is a strong biological and positional candidate to contribute to type 2 diabetes susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53593.RAmoxDiNrjrOUEd51APtjnZPdMul0FX2KEmF4t26wAdyE130_provenance.
- NP53605.RApXA6R71X21QQqFgoinluhbzKqDA_-eIM73rCysE9EUg130_assertion description "[Our results failed to replicate the association initially observed and none of the mutations were present in our familial Parkinson's disease cases. These observations suggest that this gene is unlikely to play a major effect in French familial Parkinson disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53605.RApXA6R71X21QQqFgoinluhbzKqDA_-eIM73rCysE9EUg130_provenance.
- NP53606.RApx3gxTP-qFL5Sh8y94DWw9H4xFLpdFfMgUd0r58Gbs8130_assertion description "[Taken together, these data suggest that genetic alteration at the Nurr1 locus is not a significant risk factor for the development of Parkinson's disease in our large sample of familial PD patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53606.RApx3gxTP-qFL5Sh8y94DWw9H4xFLpdFfMgUd0r58Gbs8130_provenance.
- NP53610.RAuT-3LZzx8OFvqTLc4eZRMnp3q9h-OwlmqDMC0yPGevc130_assertion description "[Identification of these polymorphisms may aid future candidate gene studies in disorders with altered dopamine signaling, such as schizophrenia Parkinson's disease and ADHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53610.RAuT-3LZzx8OFvqTLc4eZRMnp3q9h-OwlmqDMC0yPGevc130_provenance.
- NP53620.RAqakERo6lt9p2Xak6-CL329Eu18G02QtJzFNY4Wq6lbc130_assertion description "[ Our data suggest that the S810L missense mutation of the mineralocorticoid receptor does not play a major role in the etiology of pregnancy-induced hypertension in a German /Turkish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53620.RAqakERo6lt9p2Xak6-CL329Eu18G02QtJzFNY4Wq6lbc130_provenance.
- NP53623.RApHNWgC6HuYuyBeJTz8W2r2Y8RQVMAMgfSocU8RCQYMs130_assertion description "[We examined whether genetic variations in the glucocorticoid receptor gene (Nuclear Receptor Subfamily 3, Group C, Member 1; NR3C1) could be associated with increased susceptibility for MDD using a whole gene-based association analysis of single nucleotide polymorphisms (SNPs).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53623.RApHNWgC6HuYuyBeJTz8W2r2Y8RQVMAMgfSocU8RCQYMs130_provenance.
- NP53625.RAldWmCorT-qp8MYZ57YgOwZbtMXgI3GQ7fQ4f3NIhDb4130_assertion description "[A mutation of the glucocorticoid receptor gene in patients with systemic lupus erythematosus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53625.RAldWmCorT-qp8MYZ57YgOwZbtMXgI3GQ7fQ4f3NIhDb4130_provenance.
- NP53626.RAvscaoyD29D7bAhElxcB70vQp0BSXgGg8XuIf98-J8q8130_assertion description "[The data suggest a role for glucocorticoid receptor variation in the underlying cause of CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53626.RAvscaoyD29D7bAhElxcB70vQp0BSXgGg8XuIf98-J8q8130_provenance.
- NP53628.RAtbVGtQwx3rHVpiCC27VsNcKrhUnAoHvAPDgy4VYnjNI130_assertion description "[Identification of polymorphisms in the human glucocorticoid receptor gene (NR3C1) in a multi-racial asthma case and control screening panel.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53628.RAtbVGtQwx3rHVpiCC27VsNcKrhUnAoHvAPDgy4VYnjNI130_provenance.
- NP53631.RAp81buKRr900V3szGsE26m5pID1iY5Jq6heKqUfPsK88130_assertion description "[Genetic variations of the NR3C1 gene in children with sporadic nephrotic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53631.RAp81buKRr900V3szGsE26m5pID1iY5Jq6heKqUfPsK88130_provenance.
- NP53636.RAhYyn4F6UOWDNv6Xts7wRzhqO1oa-HRMow73OCdXL1jY130_assertion description "[Tsp509I polymorphism in exon 2 of the glucocorticoid receptor gene in relation to obesity and cortisol secretion: cohort study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53636.RAhYyn4F6UOWDNv6Xts7wRzhqO1oa-HRMow73OCdXL1jY130_provenance.
- NP53643.RAvBvtTezX_2Vx7S2kYy3joY3uJhHM9j3qpqJRpNzcjS0130_assertion description "[The purpose of the study was to evaluate the prevalence of SHP variants among obese Danish men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53643.RAvBvtTezX_2Vx7S2kYy3joY3uJhHM9j3qpqJRpNzcjS0130_provenance.
- NP53646.RAu-AEUHXOukvCRqf9AbFHW6MU3ZEunnqDGiV0v9dn1cw130_assertion description "[In a multicenter case-control study, 490 colorectal cancer patients and 593 controls (433 matched case-control pairs) were genotyped for common polymorphisms in the cytochrome P450 (CYP1A1, CYP1A2, CYP1B1, CYP2A6, CYP2C9, CYP2C19 and CYP2D6), glutathione S-transferase (GSTM1, GSTP1 and GSTT1), sulfotransferase (SULT1A1 and SULT1A2), N-acetyl transferase 2 (NAT2), NAD(P)H:quinone oxidoreductase (NQO1), methylenetetrahydrofolate reductase (MTHFR), and microsomal epoxide hydrolase (EPHX1) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53646.RAu-AEUHXOukvCRqf9AbFHW6MU3ZEunnqDGiV0v9dn1cw130_provenance.
- NP53650.RAveWjbFpZOuTcVyBCmlRdKZCVMRLdNHLMYr5zbTYj8UY130_assertion description "[Screening of 214 single nucleotide polymorphisms in 44 candidate cancer susceptibility genes: a case-control study on gastric and colorectal cancers in the Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53650.RAveWjbFpZOuTcVyBCmlRdKZCVMRLdNHLMYr5zbTYj8UY130_provenance.
- NP53651.RAhgu3BjQ48AlIuuBaNGjkQMD7kmfHVjqtFBjTwICQ2GY130_assertion description "[A NAD(P)H:quinone oxidoreductase 1 polymorphism is a risk factor for human colon cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53651.RAhgu3BjQ48AlIuuBaNGjkQMD7kmfHVjqtFBjTwICQ2GY130_provenance.