Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP81703.RAlHwbnt1YuFWxMx4nNVjFHVudM-jrxjD89p5LXPdfLFA130_assertion description "[Asp327Asn polymorphism of sex hormone-binding globulin gene is associated with systemic lupus erythematosus incidence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81703.RAlHwbnt1YuFWxMx4nNVjFHVudM-jrxjD89p5LXPdfLFA130_provenance.
- NP81705.RAlYqp3QFXFUtX1oQQ9lt6V22yY_lnfAG9EfmFqN-4WOs130_assertion description "[Genetic analysis of Alzheimer's disease in the Uppsala Longitudinal Study of Adult Men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81705.RAlYqp3QFXFUtX1oQQ9lt6V22yY_lnfAG9EfmFqN-4WOs130_provenance.
- NP81708.RAukA7TeMRY4CPm4PdNuytYhVyNABNPg9sAPFzIPHl9Yw130_assertion description "[Polymorphisms in mitochondrial genes and prostate cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81708.RAukA7TeMRY4CPm4PdNuytYhVyNABNPg9sAPFzIPHl9Yw130_provenance.
- NP81712.RAm6asd_phr5wg65C2GpUF7-HVqLvtxmkK8naLM49XjjU130_assertion description "[Association between single nucleotide polymorphisms of surfactant protein D and allergic rhinitis in Chinese patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81712.RAm6asd_phr5wg65C2GpUF7-HVqLvtxmkK8naLM49XjjU130_provenance.
- NP81713.RAgvJ7rxq4SQxVx1wvuPNvuedCMcII4RVPUsxciuvQSlo130_assertion description "[Genetic susceptibility to distinct bladder cancer subphenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81713.RAgvJ7rxq4SQxVx1wvuPNvuedCMcII4RVPUsxciuvQSlo130_provenance.
- NP81720.RAuubeMSDI5_mgVEviUbqVBTdeN92wXLfMWfJEfaHx_kI130_assertion description "[Surfactant protein A and D gene polymorphisms and protein expression in victims of sudden infant death.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81720.RAuubeMSDI5_mgVEviUbqVBTdeN92wXLfMWfJEfaHx_kI130_provenance.
- NP81722.RAvrbPKHCOPwEG-mgB3F86EDuUw0H-AeENMqUT3hlM4JA130_assertion description "[Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81722.RAvrbPKHCOPwEG-mgB3F86EDuUw0H-AeENMqUT3hlM4JA130_provenance.
- NP81723.RAkiDXImHNjPJWRdHoxgSXUY2ztu82SA6MAocBuV1ve8w130_assertion description "[Wnt signaling genes are associated with impaired lung function in two childhood asthma cohorts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81723.RAkiDXImHNjPJWRdHoxgSXUY2ztu82SA6MAocBuV1ve8w130_provenance.
- NP81728.RAu1ANvRJSHASrXavF7Enyu2xeSRPqHm0wb3uSaTGSKPI130_assertion description "[The childhood incidence of SMA in the Swedish population is around 1 in 12,000 live births and it is unlikely that there is any founder effect involved in SMA in western Sweden.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81728.RAu1ANvRJSHASrXavF7Enyu2xeSRPqHm0wb3uSaTGSKPI130_provenance.
- NP81732.RAh6qt7zbqHEjxJ1UQKgNOLPLMZ-oaW7KcRtP1nvO_4ug130_assertion description "[Interaction between single nucleotide polymorphisms in selenoprotein P and mitochondrial superoxide dismutase determines prostate cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81732.RAh6qt7zbqHEjxJ1UQKgNOLPLMZ-oaW7KcRtP1nvO_4ug130_provenance.
- NP81733.RAqJ02uNLzsuEXtjmD7_42-ptVTza8Aib_QCKI_mJO_pc130_assertion description "[These findings might help to explain biological effects of selenium in prostate cancer development in order to overcome inconsistencies arising from former studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81733.RAqJ02uNLzsuEXtjmD7_42-ptVTza8Aib_QCKI_mJO_pc130_provenance.
- NP81735.RAhfr5zHyNzAdg8y6pJ0F4MEnBe4orWcDEK1FP2kw0hew130_assertion description "[Polymorphisms in genes involved in neurodevelopment may be associated with altered brain morphology in schizophrenia: preliminary evidence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81735.RAhfr5zHyNzAdg8y6pJ0F4MEnBe4orWcDEK1FP2kw0hew130_provenance.
- NP81738.RAkXmBDW9maHDz6VsOjXKay1NKNKCY5RjqvMpthHUqQDY130_assertion description "[Neither replication nor simulation supports a role for the axon guidance pathway in the genetics of Parkinson's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81738.RAkXmBDW9maHDz6VsOjXKay1NKNKCY5RjqvMpthHUqQDY130_provenance.
- NP81747.RAqHXNiqKcRA2syqsdu5FSbE3DRnHFfj8Oo_vK38EpGuc130_assertion description "[After adjustment using false discovery rate for multiple testing, SNP rs13873 and haplotype rs1225934-rs13873 on BMP6-TXNDC5 genes were significantly associated with schizophrenia for the deficit cluster 1 but not for the deficit cluster 2 or nondeficit cluster.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81747.RAqHXNiqKcRA2syqsdu5FSbE3DRnHFfj8Oo_vK38EpGuc130_provenance.
- NP81753.RAu_8PSTEzywC5MLZC_WIoDK0QKG-tMFh6iStXGh4rsmY130_assertion description "[Candidate gene analysis of semaphorins in patients with Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81753.RAu_8PSTEzywC5MLZC_WIoDK0QKG-tMFh6iStXGh4rsmY130_provenance.
- NP81761.RAvwu6OaiijKznU2qIruhcDKE2hkbrGHGOqh7y6YTFq4U130_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." NP81761.RAvwu6OaiijKznU2qIruhcDKE2hkbrGHGOqh7y6YTFq4U130_provenance.
- NP81766.RAhp8G_TvcBBSUuqkHihAtoBrumc2cDCJTHWEjh3BIGRY130_assertion description "[The independent risk conferred by genetic variants encoding pathways such as inflammation and lipid metabolism, not adequately reflected by conventional biomarkers, may identify high-risk individuals for intensified control of modifiable risk factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81766.RAhp8G_TvcBBSUuqkHihAtoBrumc2cDCJTHWEjh3BIGRY130_provenance.
- NP81771.RAjkV5HZqnqDWBUQP98CTq1RpBZUqJwC7zLDYC32tlCJ8130_assertion description "[We found an association of inflammatory bowel disease with allele L206 of L-selectin gene, whereas genotype L/F was associated with a subgroup of UC (left-sided type) and CD patients with more extensive location of disease and stricturing behavior.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81771.RAjkV5HZqnqDWBUQP98CTq1RpBZUqJwC7zLDYC32tlCJ8130_provenance.
- NP81772.RAtObpKY9hXjRllCtt2gL-ndzHUrDrnlyIHXZnLMCrO4c130_assertion description "[Genetic variants in apoptosis and immunoregulation-related genes are associated with risk of chronic lymphocytic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81772.RAtObpKY9hXjRllCtt2gL-ndzHUrDrnlyIHXZnLMCrO4c130_provenance.
- NP81780.RArvlHhGkaLMQw2K6d8gcsrW6irKfat3tI0KYGaFtlyt8130_assertion description "[Association of a polymorphism of the apolipoprotein E gene with chronic kidney disease in Japanese individuals with metabolic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81780.RArvlHhGkaLMQw2K6d8gcsrW6irKfat3tI0KYGaFtlyt8130_provenance.
- NP81782.RAu71OeOPVeigi-kjUAc7EKhEgrv20W3U7oNA6bWJSYRc130_assertion description "[Polymorphisms and plasma soluble levels of E-selectin in patients with chronic hepatitis B virus infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81782.RAu71OeOPVeigi-kjUAc7EKhEgrv20W3U7oNA6bWJSYRc130_provenance.
- NP81784.RAtGfFnGEuRNdqb5co2KF4xVYorieiLGGb9JMYimScJrY130_assertion description "[The genomic basis of cerebral palsy: a HuGE systematic literature review.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81784.RAtGfFnGEuRNdqb5co2KF4xVYorieiLGGb9JMYimScJrY130_provenance.
- NP81785.RAlLabxvjRvmIHCeUD5e3-uLCOBmObRV_0lW5pEX4pTYc130_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." NP81785.RAlLabxvjRvmIHCeUD5e3-uLCOBmObRV_0lW5pEX4pTYc130_provenance.
- NP81786.RAho20UMHyMZN1viv0WAq2uFGwTfnFOLy611mibz6NcmI130_assertion description "[The frequency of minor allele (R) and heterozygous (RS) genotype of E-selectin S128R polymorphism was significantly higher in the stroke patients than in the controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81786.RAho20UMHyMZN1viv0WAq2uFGwTfnFOLy611mibz6NcmI130_provenance.
- NP81792.RApQdkcIVhHaBZANkkmrBNbfcFofNS8cdkyc7Iz5ywaCQ130_assertion description "[This large prospective cohort study provides evidence that SNPs of genes encoding prototypical inflammatory molecules may be used to create multigenic models that predict stroke risk in subjects with type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81792.RApQdkcIVhHaBZANkkmrBNbfcFofNS8cdkyc7Iz5ywaCQ130_provenance.
- NP81793.RAmU-TiKkM8tvTYRLr7dNoBgNoN8UZKhCEbg1f2N7efdw130_assertion description "[Genetic susceptibility to distinct bladder cancer subphenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81793.RAmU-TiKkM8tvTYRLr7dNoBgNoN8UZKhCEbg1f2N7efdw130_provenance.
- NP81796.RAv1I-3HTRWvG8R09PEQo7Az74r3DBaCNvvHGr--_glgo130_assertion description "[There is genetic heterogeneity in CRC associations in Americans of African versus European descent.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81796.RAv1I-3HTRWvG8R09PEQo7Az74r3DBaCNvvHGr--_glgo130_provenance.
- NP81799.RAt68mjluWEfp2uSF5O8VrbRp0AsfJiGldC6MAf2hgWa8130_assertion description "[Genetic analysis of Alzheimer's disease in the Uppsala Longitudinal Study of Adult Men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81799.RAt68mjluWEfp2uSF5O8VrbRp0AsfJiGldC6MAf2hgWa8130_provenance.
- NP81800.RAvCPHRWOujrE67ym4aC0WwP6FUVFtBfrF4sCLS_FK7a0130_assertion description "[Association of variants in two vitamin e transport genes with circulating vitamin e concentrations and prostate cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81800.RAvCPHRWOujrE67ym4aC0WwP6FUVFtBfrF4sCLS_FK7a0130_provenance.
- NP81801.RAsI_gzaI5vHcPSC9VlAfhOCNIRKc6i5YQlceq5IAdDMM130_assertion description "[Pathway-based evaluation of 380 candidate genes and lung cancer susceptibility suggests the importance of the cell cycle pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81801.RAsI_gzaI5vHcPSC9VlAfhOCNIRKc6i5YQlceq5IAdDMM130_provenance.
- NP81803.RAsqkYBFU5PaEtA_rbYPE5M9NC0mdlwIYRtioH5iD2dMw130_assertion description "[Association of bone morphogenetic protein-2 gene polymorphisms with susceptibility to ossification of the posterior longitudinal ligament of the spine and its severity in Chinese patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81803.RAsqkYBFU5PaEtA_rbYPE5M9NC0mdlwIYRtioH5iD2dMw130_provenance.
- NP81805.RAhs0dNdaHELc1EUu-KgVyG2B1FrdSjlGSv8_Opah1Nuo130_assertion description "[Genetic susceptibility to distinct bladder cancer subphenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81805.RAhs0dNdaHELc1EUu-KgVyG2B1FrdSjlGSv8_Opah1Nuo130_provenance.
- NP81812.RAiUXA2a70tjJbWNuY8SxbwcEsUUhRiGqnLHN-4HQXnTE130_assertion description "[A head and neck paraganglioma was present in 97.7% of the SDHD and 87.5% of the SDHC mutation carriers, but in only 42.7% of the SDHB carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81812.RAiUXA2a70tjJbWNuY8SxbwcEsUUhRiGqnLHN-4HQXnTE130_provenance.
- NP81817.RAk9T41qR8DbFCkwEOCYmkiMdU49eOBOxLqZ7DlUQR7d0130_assertion description "[Polymorphisms in mitochondrial genes and prostate cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81817.RAk9T41qR8DbFCkwEOCYmkiMdU49eOBOxLqZ7DlUQR7d0130_provenance.
- NP81834.RAgCWN_971uYEzKOYufMc6s78jNC66PpukQl671XWw0KU130_assertion description "[SDF1-3' a gene polymorphism is associated with laryngeal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81834.RAgCWN_971uYEzKOYufMc6s78jNC66PpukQl671XWw0KU130_provenance.
- NP81835.RAta14gP7H5bR63j4_CPheA3bq41jIYsSeMHI2-3JtL0o130_assertion description "[Genetic analysis of Alzheimer's disease in the Uppsala Longitudinal Study of Adult Men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81835.RAta14gP7H5bR63j4_CPheA3bq41jIYsSeMHI2-3JtL0o130_provenance.
- NP81846.RAg4A8QsxvI_KTZvUEWrrh1xANg1jOzTwt2NysTHEU0bU130_assertion description "[Modulation of cystic fibrosis lung disease by variants in interleukin-8.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81846.RAg4A8QsxvI_KTZvUEWrrh1xANg1jOzTwt2NysTHEU0bU130_provenance.
- NP81850.RAhy98PS3GQT8KQTy_Ou1nM5Sr63_jGmrDhna1QLl_rfk130_assertion description "[We tested the hypothesis that variation in the chemokine gene CXCL5, which encodes epithelial neutrophil-activating peptide (ENA-78), is associated with ACS prognosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81850.RAhy98PS3GQT8KQTy_Ou1nM5Sr63_jGmrDhna1QLl_rfk130_provenance.
- NP81852.RAnoCsz61EtrVfBYftecJ5x819SQamUf_lA5m98bvM41o130_assertion description "[Association of cytokine and chemokine gene polymorphisms with severe acute respiratory syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81852.RAnoCsz61EtrVfBYftecJ5x819SQamUf_lA5m98bvM41o130_provenance.
- NP81853.RAp_i9w2HTyV4ZoD5ng3M7kNQrb72RM2S1GvqCG5kr6Ek130_assertion description "[Since the presence of the rs2304052 C allele is associated with an increased risk (odds ratio: 2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81853.RAp_i9w2HTyV4ZoD5ng3M7kNQrb72RM2S1GvqCG5kr6Ek130_provenance.
- NP81859.RAkZk-Bx2hN2KSPAEnZKOtm-sU5pNZFfu7aXwIgDSr258130_assertion description "[Association of RANTES gene promoter -28C/G polymorphism with respiratory syncytial virus bronchiolitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81859.RAkZk-Bx2hN2KSPAEnZKOtm-sU5pNZFfu7aXwIgDSr258130_provenance.
- NP81864.RAsejh8dbD9xMluMAsKefg74BpbrRSzWFCMfg9S2CZ-MQ130_assertion description "[Association of genetic variants with chronic kidney disease in individuals with different lipid profiles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81864.RAsejh8dbD9xMluMAsKefg74BpbrRSzWFCMfg9S2CZ-MQ130_provenance.
- NP81865.RAnAcuFMp-zhJDG4tbKFU8QS7JRLCdZArw0vJaBV-fnTc130_assertion description "[Genetic susceptibility to distinct bladder cancer subphenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81865.RAnAcuFMp-zhJDG4tbKFU8QS7JRLCdZArw0vJaBV-fnTc130_provenance.
- NP81867.RAi-HwCxRi1CZAOiJDjoMdBhQZ8zX-n0IrXnD6quj2bfQ130_assertion description "[Independent effects of genetic variations in mannose-binding lectin influence the course of HIV disease: the advantage of heterozygosity for coding mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81867.RAi-HwCxRi1CZAOiJDjoMdBhQZ8zX-n0IrXnD6quj2bfQ130_provenance.
- NP81875.RAqNgQcm-24mTcWbUoOU0Pv5gTuyNAkiVbEf2JQLxvbOs130_assertion description "[Polymorphisms in the estrogen receptor 1 and vitamin C and matrix metalloproteinase gene families are associated with susceptibility to lymphoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81875.RAqNgQcm-24mTcWbUoOU0Pv5gTuyNAkiVbEf2JQLxvbOs130_provenance.
- NP81879.RAriH4dRIAB-Dt9IVEhQ-oOOST1EzErPClt4atxCd-_2I130_assertion description "[The MCP-1-2518 AA genotype of the population in Suzhou may be a protective genotype of AP, while one with higher frequency of G allele is more likely to suffer from pancreatitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81879.RAriH4dRIAB-Dt9IVEhQ-oOOST1EzErPClt4atxCd-_2I130_provenance.
- NP81880.RAunUm1YcfFlAqKOZkCGMnsDMvcJdtzCREGdQJ3Qb3Jh0130_assertion description "[The present study showed a significant and independent association between the -2518G/A polymorphism of the MCP-1 gene (presence of G allele) and hypertension in the Tunisian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81880.RAunUm1YcfFlAqKOZkCGMnsDMvcJdtzCREGdQJ3Qb3Jh0130_provenance.
- NP81888.RApJy49RUr6QHN84kkwDzUeT0mMmUJg1_OVW0Npa_R50M130_assertion description "[Association of cytokine and chemokine gene polymorphisms with severe acute respiratory syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81888.RApJy49RUr6QHN84kkwDzUeT0mMmUJg1_OVW0Npa_R50M130_provenance.
- NP81890.RAiphdy6yphWjj1WTAvq2YTB-cevTb43-SwRILk_q4Guk130_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." NP81890.RAiphdy6yphWjj1WTAvq2YTB-cevTb43-SwRILk_q4Guk130_provenance.
- NP81891.RAuMhWj9f_P6sPKJXoKByo2d0c1r70WBZXeg5UhD1EFgg130_assertion description "[The 47A polymorphism in the MnSOD gene and the -2518G polymorphism in the CCL2 gene are associated with the development of AU in HLA-B27-positive and -negative Chinese patients, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81891.RAuMhWj9f_P6sPKJXoKByo2d0c1r70WBZXeg5UhD1EFgg130_provenance.
- NP81892.RAlmzx6zWFS7OUl50Kck8qPosSTgFASXHdnncdpSIU8ZA130_assertion description "[Monocyte chemoattractant protein (MCP)-1 -2518 A/G SNP in Chinese Han patients with VKH syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81892.RAlmzx6zWFS7OUl50Kck8qPosSTgFASXHdnncdpSIU8ZA130_provenance.
- NP81895.RAuaq1Sh7WRLBWYt21Ehk9qbsU6rNEZ_ZIBiHO9f0YKg0130_assertion description "[We found that the distributions of AA, AG and GG genotypes of MCP-1-2518 were significantly different in NSCLC patients compared to controls (chi(2) = 10.106, P = 0.006).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81895.RAuaq1Sh7WRLBWYt21Ehk9qbsU6rNEZ_ZIBiHO9f0YKg0130_provenance.
- NP81896.RAkwr3Qg28oKHMvxnhtGw7ItOeoNmqijW9se0cgGepdWs130_assertion description "[Genetic variants in inflammation-related genes are associated with radiation-induced toxicity following treatment for non-small cell lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81896.RAkwr3Qg28oKHMvxnhtGw7ItOeoNmqijW9se0cgGepdWs130_provenance.
- NP81902.RApLEtKato10pG1TIL_56OvQqh-248UjaCK1ePYUJINZw130_assertion description "[The independent risk conferred by genetic variants encoding pathways such as inflammation and lipid metabolism, not adequately reflected by conventional biomarkers, may identify high-risk individuals for intensified control of modifiable risk factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81902.RApLEtKato10pG1TIL_56OvQqh-248UjaCK1ePYUJINZw130_provenance.
- NP81904.RAmsagN-FlGb5ncC59i51db2spXPXia8Rw_7fiERsSync130_assertion description "[This study suggests that common genetic variants in the OR10J3 and FCER1A be strongly associated with breast cancer risk among Korean women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81904.RAmsagN-FlGb5ncC59i51db2spXPXia8Rw_7fiERsSync130_provenance.
- NP81907.RAhL3GsydP_U_aIC1oce2M55eS5Wrf8YZKnS1SLV34e_4130_assertion description "[The genomic basis of cerebral palsy: a HuGE systematic literature review.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81907.RAhL3GsydP_U_aIC1oce2M55eS5Wrf8YZKnS1SLV34e_4130_provenance.
- NP81908.RAgTm6nqT703HBjhEvySAVthzgp8NJLIJN5AjpWGVyIwc130_assertion description "[The CFTR gene was first analyzed in all patients by denaturing high-performance liquid chromatography followed by direct sequencing; whereas, the sodium channel non-voltage-gated 1 alpha (SCNN1A), sodium channel non-voltage-gated 1 beta (SCNN1B), and sodium channel non-voltage-gated 1 gamma (SCNN1G) subunits of the ENaC gene were analyzed by sequencing in the five patients who carried only one CF mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81908.RAgTm6nqT703HBjhEvySAVthzgp8NJLIJN5AjpWGVyIwc130_provenance.
- NP81910.RAp1200Puy2krcMjFRRnj0MOwQHARKqpU6grme3yHoEUw130_assertion description "[The independent risk conferred by genetic variants encoding pathways such as inflammation and lipid metabolism, not adequately reflected by conventional biomarkers, may identify high-risk individuals for intensified control of modifiable risk factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81910.RAp1200Puy2krcMjFRRnj0MOwQHARKqpU6grme3yHoEUw130_provenance.
- NP81919.RAq7voDp1rMbRCHQr9IMyVsbrGYRZLp2jDggq6Sz2_H4I130_assertion description "[In conclusion, the G298S-SCN5A missense mutation caused a marked reduction of whole cell Na(+) current and loss of function of Na(v)1.5, suggesting SCN5A as a candidate gene in the pathophysiology of IBS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81919.RAq7voDp1rMbRCHQr9IMyVsbrGYRZLp2jDggq6Sz2_H4I130_provenance.
- NP81921.RAoDRBIiWmC91L3h5fnJkeU6af7BXmeXzJFrPkUwd5iuo130_assertion description "[In tandem analysis of CLCN1 and SCN4A greatly enhances mutation detection in families with non-dystrophic myotonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81921.RAoDRBIiWmC91L3h5fnJkeU6af7BXmeXzJFrPkUwd5iuo130_provenance.
- NP81923.RAjZq5sVe-STl4_xwzcf0kJnIYLh64_3LdCidydcW5uI8130_assertion description "[Sporadic infantile epileptic encephalopathy caused by mutations in PCDH19 resembles Dravet syndrome but mainly affects females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81923.RAjZq5sVe-STl4_xwzcf0kJnIYLh64_3LdCidydcW5uI8130_provenance.
- NP81925.RAgMQfZeKcAR7pL1SV1WfrtL74fopbYnCfU_LR2nPxE7g130_assertion description "[Genetic variants of BLM interact with RAD51 to increase breast cancer susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81925.RAgMQfZeKcAR7pL1SV1WfrtL74fopbYnCfU_LR2nPxE7g130_provenance.
- NP81926.RAg-mEHxZVxfXHTYy7R1Qm7UH0OnRjE9G1FQP3ItvIGdU130_assertion description "[A polymorphism in Werner syndrome gene is associated with breast cancer susceptibility in Chinese women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81926.RAg-mEHxZVxfXHTYy7R1Qm7UH0OnRjE9G1FQP3ItvIGdU130_provenance.
- NP81928.RAsXdaQEwJiE0BepgNeKQ_495TRSWb0W4_GPX2kX0K_6I130_assertion description "[Pathway-based evaluation of 380 candidate genes and lung cancer susceptibility suggests the importance of the cell cycle pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81928.RAsXdaQEwJiE0BepgNeKQ_495TRSWb0W4_GPX2kX0K_6I130_provenance.
- NP81932.RAkFUQUSDcf8uCidKN5gGoMCKPbtQeHyEU_BUfVWcbG4k130_assertion description "[Large-scale evaluation of candidate genes identifies associations between DNA repair and genomic maintenance and development of benzene hematotoxicity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81932.RAkFUQUSDcf8uCidKN5gGoMCKPbtQeHyEU_BUfVWcbG4k130_provenance.
- NP81934.RAtf8Vw9zVlUh-PKcpieDSPLjM3FvZYPXPsNzhPlwaTYc130_assertion description "[Association of genetic variants with chronic kidney disease in individuals with different lipid profiles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81934.RAtf8Vw9zVlUh-PKcpieDSPLjM3FvZYPXPsNzhPlwaTYc130_provenance.
- NP81938.RAslJWrV7-lLCz77oghFuIuwTW6iPWozPJmJwt4bz7Ibw130_assertion description "[Replication of the association between the C8orf13-BLK region and systemic lupus erythematosus in a Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81938.RAslJWrV7-lLCz77oghFuIuwTW6iPWozPJmJwt4bz7Ibw130_provenance.
- NP81944.RAvmJI41fL9LDdN19yVpesU5Ojct5Nj4UD6TlhltXlajU130_assertion description "[Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81944.RAvmJI41fL9LDdN19yVpesU5Ojct5Nj4UD6TlhltXlajU130_provenance.
- NP81945.RAmItBmSoYvV7Iz5JoVUawiPHeIhIdQIWVi7m39rS10so130_assertion description "[Genetic analysis of Alzheimer's disease in the Uppsala Longitudinal Study of Adult Men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81945.RAmItBmSoYvV7Iz5JoVUawiPHeIhIdQIWVi7m39rS10so130_provenance.
- NP81950.RAuxzVdjIUoXJ3ky6xd7XLzgs9_powfhZBstPuix8z4VY130_assertion description "[Although we did not identify variants leading to novel amino acid substitutions, nonsense or frameshift mutations, this study warrants further examination of variation in the ATXN2 gene in obesity and related phenotypes in a larger case-control study with emphasis on rs695872 and CAG repeat structure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81950.RAuxzVdjIUoXJ3ky6xd7XLzgs9_powfhZBstPuix8z4VY130_provenance.
- NP81951.RAvODeAFfEQd-WhBOAIB0bsd_vC3MGi70l-J6lIba8LTY130_assertion description "[Genome-wide association study of blood pressure and hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81951.RAvODeAFfEQd-WhBOAIB0bsd_vC3MGi70l-J6lIba8LTY130_provenance.
- NP81955.RAu_a4ofNfKcbB9aY_Wlq2pJKtoIG6gq2ujSAc0ba6vm8130_assertion description "[Human SA gene polymorphisms are associated with non-high-density lipoprotein cholesterol in postmenopausal women: a pilot study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81955.RAu_a4ofNfKcbB9aY_Wlq2pJKtoIG6gq2ujSAc0ba6vm8130_provenance.
- NP81956.RAmaBb6RTLNaSDRNijJc9Z9StM0WKBgjceoJalABv16zE130_assertion description "[High-density SNP screening of the major histocompatibility complex in systemic lupus erythematosus demonstrates strong evidence for independent susceptibility regions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81956.RAmaBb6RTLNaSDRNijJc9Z9StM0WKBgjceoJalABv16zE130_provenance.
- NP81960.RAv_wucyKEw_AoOjunP-qqib0VChjVIxszC556aL5OMyk130_assertion description "[Polymorphisms in the estrogen receptor 1 and vitamin C and matrix metalloproteinase gene families are associated with susceptibility to lymphoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81960.RAv_wucyKEw_AoOjunP-qqib0VChjVIxszC556aL5OMyk130_provenance.
- NP81970.RArXUKInaJuvoMBDULeQXMj1TSHxlH_tGps5Cm3Ba8ElY130_assertion description "[our data provide persuasive evidence against an overall association between invasive breast cancer risk and ERCC4 rs744154, TNF rs361525, CASP10 rs13010627, PGR rs1042838, and BID rs8190315 genotypes among women of European descent.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81970.RArXUKInaJuvoMBDULeQXMj1TSHxlH_tGps5Cm3Ba8ElY130_provenance.
- NP81971.RAv6IIkeGCU6AobdTxqMGoO-dgYRTobc3J88rFJ79J55o130_assertion description "[This is the first study describing genetic variation, associated with allergy, in S100A7.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81971.RAv6IIkeGCU6AobdTxqMGoO-dgYRTobc3J88rFJ79J55o130_provenance.
- NP81979.RArWfzp4XNSvP7oSYz-56xrCaQ_oI-PkzqjXgSj8j9O2o130_assertion description "[our data suggest a genetic and functional association of PBX1 with BMD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81979.RArWfzp4XNSvP7oSYz-56xrCaQ_oI-PkzqjXgSj8j9O2o130_provenance.
- NP81985.RAh-CexxoFSx5iV8Pe9e-Kp1WcP10TIjfTqI4BS4UB6Bo130_assertion description "[A major genomic region involved in Wegener's granulomatosis includes the gene for retinoid receptor beta (RXRB) which forms heterodimers with peroxisome proliferator-activated receptors (PPARs).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81985.RAh-CexxoFSx5iV8Pe9e-Kp1WcP10TIjfTqI4BS4UB6Bo130_provenance.
- NP81987.RAp-10qZXUj1HYttCcAhOLTDhqK4bzllLVeEi9rRgifSk130_assertion description "[Genetic susceptibility to distinct bladder cancer subphenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81987.RAp-10qZXUj1HYttCcAhOLTDhqK4bzllLVeEi9rRgifSk130_provenance.
- NP81990.RArAM5qZYjMCdhS8GqxC6hczwsin2S2gtHkXbYkOWpgJg130_assertion description "[One of the identified seven SNPs in RXRA influenced AD risk in our single marker analysis (rs3132293: P= 0.006).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81990.RArAM5qZYjMCdhS8GqxC6hczwsin2S2gtHkXbYkOWpgJg130_provenance.
- NP81994.RAk9jYTxSmWnCgdmr3sdJDGt77binuTfqBbVdF72j1vog130_assertion description "[PTEN identified as important risk factor of chronic obstructive pulmonary disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81994.RAk9jYTxSmWnCgdmr3sdJDGt77binuTfqBbVdF72j1vog130_provenance.
- NP81997.RAsnJKXZxOdBwOXXO9hwYro3rt4vthyNxMCLcTgLK8kGM130_assertion description "[To examine whether the novel promoter variant in RUNX2 is associated with the risk of T2DM and related phenotypes, RUNX2-742G > T was genotyped in 378 T2DM patients and 382 normal controls recruited in the Korean T2DM Study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81997.RAsnJKXZxOdBwOXXO9hwYro3rt4vthyNxMCLcTgLK8kGM130_provenance.
- NP81998.RAmhWkQUIzwmZIYUQZHGP2pA1ROuA0M6L9dBcmX4alUYo130_assertion description "[Our study results revealed that the RUNX3 intronic T/A polymorphism (rs760805) might modulate the risk of gastric atrophy among H. pylori seropositive subjects, and the RUNX3 T/A polymorphism at exon 1 (rs6672420) had little influence on the risks of H. pylori infection, gastric atrophy or gastric cancer in Japanese people.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81998.RAmhWkQUIzwmZIYUQZHGP2pA1ROuA0M6L9dBcmX4alUYo130_provenance.
- NP82002.RAt8yxVl0g7bcvob5VjPe6nvzDimlyDUO0hCFmUdixQcI130_assertion description "[This study showed for the first time a high frequency of RUNX1 mutations in CMML.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP82002.RAt8yxVl0g7bcvob5VjPe6nvzDimlyDUO0hCFmUdixQcI130_provenance.
- NP82004.RAhcNPQ5wI1cShNtNwDR5Hwk5pKlknadTXDIkJAGI8mvE130_assertion description "[Two-stage case-control association study of polymorphisms in rheumatoid arthritis susceptibility genes with schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP82004.RAhcNPQ5wI1cShNtNwDR5Hwk5pKlknadTXDIkJAGI8mvE130_provenance.
- NP82005.RAl1vLH-i78U7PH4EHWSKcG84G4o5zbVolPHgvJOuwH74130_assertion description "[These point towards a variety of candidate genes that could contribute to the pathogenesis of minimally differentiated acute myeloid leukemia, including the tumor suppressor genes TP53 and NF1, and reinforced the importance of RUNX1 in this leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP82005.RAl1vLH-i78U7PH4EHWSKcG84G4o5zbVolPHgvJOuwH74130_provenance.
- NP82010.RAknh8iq9YNJCfvdwHZ7Ve5qmtsppWFEY9SikSrWk98jc130_assertion description "[Pathway-based evaluation of 380 candidate genes and lung cancer susceptibility suggests the importance of the cell cycle pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP82010.RAknh8iq9YNJCfvdwHZ7Ve5qmtsppWFEY9SikSrWk98jc130_provenance.
- NP82012.RAvwyA-7p6uHKUJW4qHMK1waSZzcOU4HIkYBmD0UJlwT0130_assertion description "[Transmission disequilibrium of SNP alleles in cystathionine-beta-synthase, dihydrofolate reductase, methylenetetrahydrofolate reductase, and thymidylate synthetase confers an increased susceptibility to SB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP82012.RAvwyA-7p6uHKUJW4qHMK1waSZzcOU4HIkYBmD0UJlwT0130_provenance.
- NP82017.RArBQajeQm9UxwjwfnzGD_TPdq7sNuXRMFXfO8b1rI5MM130_assertion description "[Germline polymorphisms in the one-carbon metabolism pathway and DNA methylation in colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP82017.RArBQajeQm9UxwjwfnzGD_TPdq7sNuXRMFXfO8b1rI5MM130_provenance.
- NP82018.RAkC0SuD9Tewj6lrOgFR2KOHl6KGmmIkAQNAXfFVWbEZY130_assertion description "[Single nucleotide polymorphisms of gemcitabine metabolic genes and pancreatic cancer survival and drug toxicity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP82018.RAkC0SuD9Tewj6lrOgFR2KOHl6KGmmIkAQNAXfFVWbEZY130_provenance.
- NP82024.RAtuO9PcRAO2yLQx9WGwloD70AZptSuqG8ArxvsA-2Iqg130_assertion description "[The association between osteocalcin gene polymorphism and dental fluorosis among children exposed to fluoride in People's Republic of China.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP82024.RAtuO9PcRAO2yLQx9WGwloD70AZptSuqG8ArxvsA-2Iqg130_provenance.
- NP82025.RAk_82ectF6MnhkuUYXCI2y317DvxcIItovDAm0R0ZKx4130_assertion description "[In this genotype-phenotype analysis we screened the coding sequence and intron-exon boundaries of RPS14, RPS16, RPS24, RPL5, RPL11, and RPL35A in 92 Italian patients with Diamond-Blackfan anemia who were negative for RPS19 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP82025.RAk_82ectF6MnhkuUYXCI2y317DvxcIItovDAm0R0ZKx4130_provenance.
- NP82032.RApgqlH5cIpEt1AA0tX040UxExRVvC0ZAX0W46v559jlg130_assertion description "[we provide evidence for a role of genetic variation in complement genes, particularly C5 and C9, and NHL risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP82032.RApgqlH5cIpEt1AA0tX040UxExRVvC0ZAX0W46v559jlg130_provenance.
- NP82034.RAuvxAx_S1ZVlW18WznVinvKQ5ddk0IF2PQKOyKCdPeQ4130_assertion description "[Although differences between individual families can only be suggested, the aggregate results in multiplex families demonstrate effect sizes that are increased as compared with those reported in previous studies for sporadic cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP82034.RAuvxAx_S1ZVlW18WznVinvKQ5ddk0IF2PQKOyKCdPeQ4130_provenance.
- NP82040.RAvlf6WdLqtJ9CuZM1h3E_2pV8rNeOGJI7_UdRHDl15v8130_assertion description "[Tag-SNP analysis of the GFI1-EVI5-RPL5-FAM69 risk locus for multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP82040.RAvlf6WdLqtJ9CuZM1h3E_2pV8rNeOGJI7_UdRHDl15v8130_provenance.
- NP82043.RAlH9gAlIfAxBn3C0k-d2Em1UqbO_oPHbJkH0tiD5qIlw130_assertion description "[Investigation of the functional brain-derived neurotrophic factor gene variant Val66MET in migraine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP82043.RAlH9gAlIfAxBn3C0k-d2Em1UqbO_oPHbJkH0tiD5qIlw130_provenance.
- NP82045.RAhhG4B9y7DlGWhn8iu4fnOJ-EyU3M9lVEio3E9RzkA8w130_assertion description "[Brain derived neurotrophic factor Val66Met polymorphism, the five factor model of personality and hippocampal volume: Implications for depressive illness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP82045.RAhhG4B9y7DlGWhn8iu4fnOJ-EyU3M9lVEio3E9RzkA8w130_provenance.
- NP82047.RAnm61AoKfoPAYpCpLW_KoaxOKAbo08FE-eT1kqKjkBrI130_assertion description "[The low number of studies on this topic and their limited sample size, along with the inner limits in the definition of anxiety phenotypes, suggest caution in the interpretation of these results.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP82047.RAnm61AoKfoPAYpCpLW_KoaxOKAbo08FE-eT1kqKjkBrI130_provenance.
- NP82050.RAsg3WDu55dv4sDpH6i7Tswoj8AtXeiIL626YuZOh6N8E130_assertion description "[Correlation of a set of gene variants, life events and personality features on adult ADHD severity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP82050.RAsg3WDu55dv4sDpH6i7Tswoj8AtXeiIL626YuZOh6N8E130_provenance.
- NP82051.RAiRfGPGWEpAkcPy9SYeFWOb9D7bDIsi1HVCSGN_YXqro130_assertion description "[Gene-gene interactions among CHRNA4, CHRNB2, BDNF, and NTRK2 in nicotine dependence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP82051.RAiRfGPGWEpAkcPy9SYeFWOb9D7bDIsi1HVCSGN_YXqro130_provenance.