Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP80863.RAqr0ZD-jIVKtvamNmoQDxeu7yZ1qG1nf3Vu4LzLgGGrs130_assertion description "[Association of transforming growth factor-beta1 single nucleotide polymorphism C-509T with allergy and immunological activities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80863.RAqr0ZD-jIVKtvamNmoQDxeu7yZ1qG1nf3Vu4LzLgGGrs130_provenance.
- NP80864.RAtxULB8AVh_TjT6q5jUesUgZduySvbq3ydOmFJi0MQyw130_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." NP80864.RAtxULB8AVh_TjT6q5jUesUgZduySvbq3ydOmFJi0MQyw130_provenance.
- NP80868.RAq6xmVM_yADSmLa7xO1WooSww6ZJkUSV8i2TntiVwPIc130_assertion description "[support a role for TGFB1 in AD pathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80868.RAq6xmVM_yADSmLa7xO1WooSww6ZJkUSV8i2TntiVwPIc130_provenance.
- NP80870.RAnj6PVj2cVkBiAesrbwZF022f_Zg6MWEdUfe3HGa1yWE130_assertion description "[Low frequency of CD4+CD25+ Treg in SLE patients: a heritable trait associated with CTLA4 and TGFbeta gene variants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80870.RAnj6PVj2cVkBiAesrbwZF022f_Zg6MWEdUfe3HGa1yWE130_provenance.
- NP80871.RArHwrCZyetVIYmL0x5_TcrkIpCAkH1gb7QtWPzWkYxFQ130_assertion description "[We have identified a SNP in the TGFB1 (transforming growth factor beta 1) gene that is associated with susceptibility to otosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80871.RArHwrCZyetVIYmL0x5_TcrkIpCAkH1gb7QtWPzWkYxFQ130_provenance.
- NP80872.RAhG83S-IXiYf5Vd6WQ77kE3ZQPTUG1ZEQ0UVbJA5FYqk130_assertion description "[On the basis of very low P-values, replication in an independent population and a functional effect of the protective variant, we conclude that TGF-beta1 influences the susceptibility for otosclerosis, and that the I263 variant is protective against the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80872.RAhG83S-IXiYf5Vd6WQ77kE3ZQPTUG1ZEQ0UVbJA5FYqk130_provenance.
- NP80878.RApg3BpxskqNu2ZfbK6EF3pqkFnfq1qKXTPbe7llmZDQ4130_assertion description "[Assessment of 14 functional gene polymorphisms in Japanese patients with oral lichen planus: a pilot case-control study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80878.RApg3BpxskqNu2ZfbK6EF3pqkFnfq1qKXTPbe7llmZDQ4130_provenance.
- NP80881.RAt3MY4Z2GkWLF8Gvprz9syX7_W2bkqO-czCTVFzUa0hY130_assertion description "[The -509C/T polymorphism of transforming growth factor-beta1 is associated with increased risk for development of chronic idiopathic neutropenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80881.RAt3MY4Z2GkWLF8Gvprz9syX7_W2bkqO-czCTVFzUa0hY130_provenance.
- NP80886.RAgzzSavuKR20ZZLil6VlWlfJh2MsCk_rcS7LwkUUFHig130_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." NP80886.RAgzzSavuKR20ZZLil6VlWlfJh2MsCk_rcS7LwkUUFHig130_provenance.
- NP80897.RAocRdjz5J5gWuU9llxLhbyiUrOraCdEkCCdFgcpbwhyc130_assertion description "[Genetic susceptibility to distinct bladder cancer subphenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80897.RAocRdjz5J5gWuU9llxLhbyiUrOraCdEkCCdFgcpbwhyc130_provenance.
- NP80905.RAoIneb7MfdRJ1XbwXLiosBAdONzE60BI7QgskbIbmz7E130_assertion description "[Genetic susceptibility to distinct bladder cancer subphenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80905.RAoIneb7MfdRJ1XbwXLiosBAdONzE60BI7QgskbIbmz7E130_provenance.
- NP80908.RAv8LtK9sewYR_H9Rc6ceNjwVyG5I12DZixvJTmFBD6Gc130_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." NP80908.RAv8LtK9sewYR_H9Rc6ceNjwVyG5I12DZixvJTmFBD6Gc130_provenance.
- NP80910.RAtAyrFMEs9fL2xUhRX_SMeLDeRVGVg-aq2RMAnkJg6nA130_assertion description "[The variants near TFAP2B appear to influence central adiposity through an effect on overall obesity/fat-mass, whereas LYPLAL1 displays a strong female-only association with fat distribution.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80910.RAtAyrFMEs9fL2xUhRX_SMeLDeRVGVg-aq2RMAnkJg6nA130_provenance.
- NP80914.RAoanzIUk5P46qcGDMFItEzyOiSQ9nf5ZImkz6-0b9c4A130_assertion description "[Mitochondrial transcription factor A variants and the risk of Parkinson's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80914.RAoanzIUk5P46qcGDMFItEzyOiSQ9nf5ZImkz6-0b9c4A130_provenance.
- NP80915.RAjaUNPkehDmdWq0n9guotbtFa0OqLPf8oRNIzzW_jiTc130_assertion description "[Mitochondrial transcription factor A (TFAM) gene variation in Parkinson's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80915.RAjaUNPkehDmdWq0n9guotbtFa0OqLPf8oRNIzzW_jiTc130_provenance.
- NP80919.RAsErjJHxgaG0uyZ2cpfLkC35YTPdw-PH5nCXCuRhEUeU130_assertion description "[A significant fraction of individuals with pulmonary fibrosis have short telomere lengths that cannot be explained by coding mutations in telomerase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80919.RAsErjJHxgaG0uyZ2cpfLkC35YTPdw-PH5nCXCuRhEUeU130_provenance.
- NP80922.RApxuKt5lgbGsteMuPaeYQF0Z9GW40lF9yuU1xGMwrtwI130_assertion description "[The susceptibility region contains two genes, TERT and CLPTM1L, suggesting that one or both may have a role in lung cancer etiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80922.RApxuKt5lgbGsteMuPaeYQF0Z9GW40lF9yuU1xGMwrtwI130_provenance.
- NP80925.RApkvZkI-fPCT6VVfyr2XXKBzDvVh_P3SWE9EGmwQwcyc130_assertion description "[Role of 5p15.33 (TERT-CLPTM1L), 6p21.33 and 15q25.1 (CHRNA5-CHRNA3) variation and lung cancer risk in never-smokers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80925.RApkvZkI-fPCT6VVfyr2XXKBzDvVh_P3SWE9EGmwQwcyc130_provenance.
- NP80934.RAqe_LjRDtf89R27_8uxo1CDXFlUR9_8mXu3RuXj7rBXE130_assertion description "[Four SNPs in the TERT and POT1 genes were significantly related with overall breast cancer risk. This initial analysis provides valuable clues for further exploration of the biological role of telomere pathway genes in breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80934.RAqe_LjRDtf89R27_8uxo1CDXFlUR9_8mXu3RuXj7rBXE130_provenance.
- NP80937.RAl_1c8C1mu813hkn-quAj-mpvEbNxarLaSFyGDC2efeo130_assertion description "[Genetic variations on chromosomes 5p15 and 15q25 and bladder cancer risk: findings from the Los Angeles-Shanghai bladder case-control study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80937.RAl_1c8C1mu813hkn-quAj-mpvEbNxarLaSFyGDC2efeo130_provenance.
- NP80938.RAveMfxD3jFKWG7YfbDc-Sz5kHBG0zCyWk9itEst-rb3E130_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." NP80938.RAveMfxD3jFKWG7YfbDc-Sz5kHBG0zCyWk9itEst-rb3E130_provenance.
- NP80940.RAvwTunhVbqepniSsWEdjHJaAbbzvSXuZBHqKy_aMx9Tw130_assertion description "[Chromosome 7p11.2 (EGFR) variation influences glioma risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80940.RAvwTunhVbqepniSsWEdjHJaAbbzvSXuZBHqKy_aMx9Tw130_provenance.
- NP80948.RAk-xdt7ZfaptK1M_0oL5FbHQRZBnd-z4CMKn-LAN4mbY130_assertion description "[Polymorphisms in telomere-associated genes, breast cancer susceptibility and prognosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80948.RAk-xdt7ZfaptK1M_0oL5FbHQRZBnd-z4CMKn-LAN4mbY130_provenance.
- NP80949.RAhsByyNNQx9yGjCJ4dozOhjg3Ic87VJNsgnL-Z9eBX2k130_assertion description "[Four SNPs in the TERT and POT1 genes were significantly related with overall breast cancer risk. This initial analysis provides valuable clues for further exploration of the biological role of telomere pathway genes in breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80949.RAhsByyNNQx9yGjCJ4dozOhjg3Ic87VJNsgnL-Z9eBX2k130_provenance.
- NP80955.RAjBpKQ30FKU6H9yF06bzklo5plbKUP0YLZRtD4Tubrd0130_assertion description "[Polymorphisms in telomere-associated genes, breast cancer susceptibility and prognosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80955.RAjBpKQ30FKU6H9yF06bzklo5plbKUP0YLZRtD4Tubrd0130_provenance.
- NP80958.RAncqJ0Y30NT7KWlhkO4ylPSjRzpHlDcJJ8lfj2K1wA6U130_assertion description "[Genetic susceptibility to distinct bladder cancer subphenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80958.RAncqJ0Y30NT7KWlhkO4ylPSjRzpHlDcJJ8lfj2K1wA6U130_provenance.
- NP80959.RAoaA6EP8uJ9mYU_ChNBOBSR64BDH5boiIBDSSSSKJVQM130_assertion description "[A significantly higher proportion of probands with familial pulmonary fibrosis (24%) and sporadic case subjects (23%) in which no coding mutation in TERT or TERC was found had telomere lengths less than the 10th percentile when compared with control subjects (P = 2.6 x 10(-8)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80959.RAoaA6EP8uJ9mYU_ChNBOBSR64BDH5boiIBDSSSSKJVQM130_provenance.
- NP80964.RAgeCXV35KWPveWnS73-Sd6vcXx56vq3HXGOkQ9ro5eNY130_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." NP80964.RAgeCXV35KWPveWnS73-Sd6vcXx56vq3HXGOkQ9ro5eNY130_provenance.
- NP80965.RAjRupEr_SnLItnBWaNF8o6ZaQTnq0tze0VT5uHoMtRi8130_assertion description "[Polymorphisms in telomere-associated genes, breast cancer susceptibility and prognosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80965.RAjRupEr_SnLItnBWaNF8o6ZaQTnq0tze0VT5uHoMtRi8130_provenance.
- NP80967.RAjSbO9Fl2liYjuKX25WHGR3ecoJ3k72IaouoIoJJ7jc0130_assertion description "[Genetic susceptibility to distinct bladder cancer subphenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80967.RAjSbO9Fl2liYjuKX25WHGR3ecoJ3k72IaouoIoJJ7jc0130_provenance.
- NP80969.RAiuoBwSX67oEKKvBRbirEcbKVHW8d6dHRjPG1R3rQAVk130_assertion description "[Somatic mutations in angiopoietin receptor gene TEK cause solitary and multiple sporadic venous malformations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80969.RAiuoBwSX67oEKKvBRbirEcbKVHW8d6dHRjPG1R3rQAVk130_provenance.
- NP80972.RAkwpuRupvPBHu26AatwzyhpSTFvoegjXe9Pe_5LOOfeo130_assertion description "[Excess maternal transmission of markers in TCOF1 among cleft palate case-parent trios from three populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80972.RAkwpuRupvPBHu26AatwzyhpSTFvoegjXe9Pe_5LOOfeo130_provenance.
- NP80974.RAp5CxI5G57asiPtpQwqPmmLzGeF7V1p1wMr1E_P6sIw8130_assertion description "[Genetic susceptibility to distinct bladder cancer subphenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80974.RAp5CxI5G57asiPtpQwqPmmLzGeF7V1p1wMr1E_P6sIw8130_provenance.
- NP80975.RAleFqVTt8OSFWIFzZyUtstQ7XKWwTgH25uvBp72Rx85k130_assertion description "[High-throughput multiplex single-nucleotide polymorphism (SNP) analysis in genes involved in methionine metabolism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80975.RAleFqVTt8OSFWIFzZyUtstQ7XKWwTgH25uvBp72Rx85k130_provenance.
- NP80977.RAlDS79ZvM3fVHD0WnzckG0phfDEb_zqxI9D0XvW_B7Xo130_assertion description "[Caucasian patients (n = 255) treated at two German hospitals for intracranial aneurysms and local controls (n = 348) were genotyped for the following polymorphisms: methionine synthase (MTR) c.2756A-->G, methylenetetrahydrofolate reductase (MTHFR) c.677C-->T, MTHFR c.1298A-->C, cystathionine beta-synthase (CBS) c.844_855ins68, CBS c.833T-->C, dihydrofolate reductase (DHFR) c.594 + 59del19bp, glutathione S-transferase Omega-1 (GSTO1) c.428C-->A, reduced folate carrier 1 (RFC1) c.80G-->A and transcobalamin 2 (Tc2) c.776C-->G.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80977.RAlDS79ZvM3fVHD0WnzckG0phfDEb_zqxI9D0XvW_B7Xo130_provenance.
- NP80978.RAuuW_N1uDt2rOvJVXy4yVQUCPk2lrIOBx9buYFEr-JTA130_assertion description "[A80G polymorphism of reduced folate carrier 1 (RFC1) and C776G polymorphism of transcobalamin 2 (TC2) genes in Down's syndrome etiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80978.RAuuW_N1uDt2rOvJVXy4yVQUCPk2lrIOBx9buYFEr-JTA130_provenance.
- NP80982.RAipCjhSDi9MoZh2Q4i-2rDBp8QAG3VeJQzWx87eF9wmc130_assertion description "[Variants of folate metabolism genes and risk of left-sided cardiac defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80982.RAipCjhSDi9MoZh2Q4i-2rDBp8QAG3VeJQzWx87eF9wmc130_provenance.
- NP80985.RAi2n1adPized6ZQAAMMEnvmBTo6v8Zf33BFMrRowYEp0130_assertion description "[Transcription factor 7-like 2 polymorphism and colon cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80985.RAi2n1adPized6ZQAAMMEnvmBTo6v8Zf33BFMrRowYEp0130_provenance.
- NP80986.RAqJIJf_u1051Aw2-erHre-D0HtuyWk2174jNAt8kOhWA130_assertion description "[the marginal association of the TCF7L2 SNP with CRC might be due to chance, but warrants further laboratory and epidemiological investigation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80986.RAqJIJf_u1051Aw2-erHre-D0HtuyWk2174jNAt8kOhWA130_provenance.
- NP80989.RAhFhceB7D8Kddzfx26nZiFOEN2R1thaTIlC9HQpz3s3E130_assertion description "[Impact of TCF7L2 rs7903146 on insulin secretion and action in young and elderly Danish twins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80989.RAhFhceB7D8Kddzfx26nZiFOEN2R1thaTIlC9HQpz3s3E130_provenance.
- NP80993.RAnIRe6YkJNrd-GrPYr6BD8caneNn1uNqt17ZAbJ-dXYU130_assertion description "[We found evidence that diabetes and obesity risk alleles interact with maternal pregravid body mass index to predict gestational weight gain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80993.RAnIRe6YkJNrd-GrPYr6BD8caneNn1uNqt17ZAbJ-dXYU130_provenance.
- NP80996.RAm7RqTYrkLYhUEH0fHVHPmpKuLRagMQZhAtG3DBOlh0s130_assertion description "[The functional relevance of TCF7L2 polymorphisms and their effects on T2D and obesity remained to be further investigated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80996.RAm7RqTYrkLYhUEH0fHVHPmpKuLRagMQZhAtG3DBOlh0s130_provenance.
- NP81004.RApUQDOhIR17iZr09nWoPx-SeMhFfCSF9oq49DCDkhaew130_assertion description "[Genetic variants of cyclin-dependent kinase 5 regulatory subunit associated protein 1-like 1 and transcription factor 7-like 2 are not associated with polycystic ovary syndrome in Chinese women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81004.RApUQDOhIR17iZr09nWoPx-SeMhFfCSF9oq49DCDkhaew130_provenance.
- NP81007.RAsG2x4kWvgKYarLmpsJnEy_7i1byr-qZn_-HxRixg7PQ130_assertion description "[Findings from bipolar disorder genome-wide association studies replicate in a Finnish bipolar family-cohort.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81007.RAsG2x4kWvgKYarLmpsJnEy_7i1byr-qZn_-HxRixg7PQ130_provenance.
- NP81008.RAu2iDb1RR24fRPA9f-U6VKO17dzBL1B4G-NSBq0je49s130_assertion description "[Phenotype-genotype interactions on renal function in type 2 diabetes: an analysis using structural equation modelling.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81008.RAu2iDb1RR24fRPA9f-U6VKO17dzBL1B4G-NSBq0je49s130_provenance.
- NP81010.RAla_wq6rRXlcGE_QVq3qUrvQXkaKdPwZa_G3PTfk60Pk130_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." NP81010.RAla_wq6rRXlcGE_QVq3qUrvQXkaKdPwZa_G3PTfk60Pk130_provenance.
- NP81013.RAsx3LD9eCNW6K6Yfi4Puz9Wwu4-h_HAm5-qbI-GDO4sU130_assertion description "[Our results confirm that common risk factors in the major histocompatibility complex region and TCF4 gene are associated with schizophrenia in Han Chinese, but our results fail to show an association with SNP rs12807809 in the NRGN gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81013.RAsx3LD9eCNW6K6Yfi4Puz9Wwu4-h_HAm5-qbI-GDO4sU130_provenance.
- NP81014.RAsx_mubqNP1FBNlouH22rEAioJXDRmh5SxJ1QYabqlWo130_assertion description "[Genome-wide association study identifies five new schizophrenia loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81014.RAsx_mubqNP1FBNlouH22rEAioJXDRmh5SxJ1QYabqlWo130_provenance.
- NP81020.RAvUh4vSE5BTl8yCmlOWrcZeOfbNAL5NGwR3TXzvRQh5M130_assertion description "[We report a novel association between the fetal ADCY5 type 2 diabetes risk allele and decreased birthweight, and confirm in meta-analyses associations between decreased birthweight and the type 2 diabetes risk alleles of HHEX-IDE and CDKAL1. No strong general effect on birthweight can be ascribed to the 25 common type 2 diabetes risk alleles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81020.RAvUh4vSE5BTl8yCmlOWrcZeOfbNAL5NGwR3TXzvRQh5M130_provenance.
- NP81021.RAsYug8g_Uus6ZY3sAioZ0L3qtf_A6J5190UmcaXPpRUo130_assertion description "[Chromosome 17q12 variants contribute to risk of early-onset prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81021.RAsYug8g_Uus6ZY3sAioZ0L3qtf_A6J5190UmcaXPpRUo130_provenance.
- NP81022.RAoFS2lIzNUIZwDzpX9-l3tfUtvR0Z6QE_2CgpT5HYrxE130_assertion description "[This study provides more stable OR estimates for PCa risk-associated SNPs, which is an important baseline for the effect of these SNPs in risk prediction. These SNPs explain a considerable proportion of genetic variance, however, the majority of genetic variance has yet to be explained.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81022.RAoFS2lIzNUIZwDzpX9-l3tfUtvR0Z6QE_2CgpT5HYrxE130_provenance.
- NP81023.RAh8PPkxf5Gz1nj43dq9UUgeT6ndX3kVh0cwOoqoFr_Qw130_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." NP81023.RAh8PPkxf5Gz1nj43dq9UUgeT6ndX3kVh0cwOoqoFr_Qw130_provenance.
- NP81024.RAloDZgCCr320JXGhoY8pNOra9w5zIHaa50_ivYTblsBc130_assertion description "[We identified and then confirmed through replication two new genetic loci for SLE: a promoter-region allele associated with reduced expression of BLK and increased expression of C8orf13 and variants in the ITGAM-ITGAX region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81024.RAloDZgCCr320JXGhoY8pNOra9w5zIHaa50_ivYTblsBc130_provenance.
- NP81026.RAmqTkTSrRIvXgtxqPh0ttGRF0NdtVsewg-QWKfnUk4og130_assertion description "[The role of Lamin A/C mutations in Danish patients with idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81026.RAmqTkTSrRIvXgtxqPh0ttGRF0NdtVsewg-QWKfnUk4og130_provenance.
- NP81033.RAhYXgdsmED_IZEpTEXOg3VihuI5MkYTxkIS2SVAFvaks130_assertion description "[Polymorphism in the IL18 gene and epithelial ovarian cancer in non-Hispanic white women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81033.RAhYXgdsmED_IZEpTEXOg3VihuI5MkYTxkIS2SVAFvaks130_provenance.
- NP81037.RAroNH_Ty_yBIvqb0wjPaNc5B5OuH0SgGR7TiPHvMdhG4130_assertion description "[Recapitulation of two genomewide association studies on blood pressure and essential hypertension in the Korean population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81037.RAroNH_Ty_yBIvqb0wjPaNc5B5OuH0SgGR7TiPHvMdhG4130_provenance.
- NP81038.RAugfsVCpEtw4ZrL9pw62ICZqaAtiSkTIeObDq96lxqk4130_assertion description "[Association of TBX5 gene polymorphism with ventricular septal defect in the Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81038.RAugfsVCpEtw4ZrL9pw62ICZqaAtiSkTIeObDq96lxqk4130_provenance.
- NP81042.RAq1n9qhqe2hqwRj49vYp912pkIl9MNqOgKY23b7mk7Bo130_assertion description "[Polymorphisms in inflammation-related genes are associated with susceptibility to major depression and antidepressant response.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81042.RAq1n9qhqe2hqwRj49vYp912pkIl9MNqOgKY23b7mk7Bo130_provenance.
- NP81043.RAgqv4IFHFgwmGPn3TzSMFfgRF2WzPNQpGu2er77bUYgA130_assertion description "[Association of TBX21 polymorphisms in a Korean population with rheumatoid arthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81043.RAgqv4IFHFgwmGPn3TzSMFfgRF2WzPNQpGu2er77bUYgA130_provenance.
- NP81046.RAieVjYl5tSLcMZJb12Fe9AK7l4eXngMTMWA_eFBkvxoY130_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." NP81046.RAieVjYl5tSLcMZJb12Fe9AK7l4eXngMTMWA_eFBkvxoY130_provenance.
- NP81049.RAhEIgfzsz0XJvvuVhzGQtNwRNra7j4wiGvE1vnQFFHf4130_assertion description "[Follow-up of a major linkage peak on chromosome 1 reveals suggestive QTLs associated with essential hypertension: GenNet study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81049.RAhEIgfzsz0XJvvuVhzGQtNwRNra7j4wiGvE1vnQFFHf4130_provenance.
- NP81050.RAsxEyspkMA2ODIFwo-aYaqTe2GEWk8OZyYxr6b5LmtYk130_assertion description "[SNPs located at the gene HUS1 are good candidates for further investigation in independent association studies and functional assays.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81050.RAsxEyspkMA2ODIFwo-aYaqTe2GEWk8OZyYxr6b5LmtYk130_provenance.
- NP81052.RAm0kYjZdfMVz-0J8ohiOgZ0LJbMZ47ypUwy6-RxlBaZA130_assertion description "[Altogether, the frequency of TARDBP gene mutations appears to be particularly high in Italian ALS patients compared to individuals of mainly Northern European origin (2.7% vs. 1%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81052.RAm0kYjZdfMVz-0J8ohiOgZ0LJbMZ47ypUwy6-RxlBaZA130_provenance.
- NP81079.RAp3PwgjNzY6xvzXtJwKRtI1GPOh5Q2qMLLgOvP-cEv4k130_assertion description "[Association of intronic polymorphism rs3773364 A>G in synapsin-2 gene with idiopathic epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81079.RAp3PwgjNzY6xvzXtJwKRtI1GPOh5Q2qMLLgOvP-cEv4k130_provenance.
- NP81083.RAgImgfOlc8Ka6_z7zo2LXpCtBWBt-GsnG30N_Tp5xyI0130_assertion description "[Bladder cancer risk and genetic variation in AKR1C3 and other metabolizing genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81083.RAgImgfOlc8Ka6_z7zo2LXpCtBWBt-GsnG30N_Tp5xyI0130_provenance.
- NP81086.RAokLArE8FXdWIeseCKo7pVui-pbl575aq6loxXqd4UBg130_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." NP81086.RAokLArE8FXdWIeseCKo7pVui-pbl575aq6loxXqd4UBg130_provenance.
- NP81095.RArsBuiLENcBmRRp-LZk92W4wjDPyFvLzWPQlOZPo0UE0130_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." NP81095.RArsBuiLENcBmRRp-LZk92W4wjDPyFvLzWPQlOZPo0UE0130_provenance.
- NP81103.RAjT3WErSghPZ9Izg1bXq2aEcetGo0cEAtseZ8f9X2v1I130_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." NP81103.RAjT3WErSghPZ9Izg1bXq2aEcetGo0cEAtseZ8f9X2v1I130_provenance.
- NP81106.RAqd7zS-yg13dAMydgAszQfZS0pe8QzaMl8jaCWqQkfwc130_assertion description "[Our findings suggest that HTR5A gene could play an important role in the pathogenesis of bipolar disorder in our population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81106.RAqd7zS-yg13dAMydgAszQfZS0pe8QzaMl8jaCWqQkfwc130_provenance.
- NP81109.RAirqHwucXOapo97g2iqkvyvSE8viNequ0LmTZeMj6Log130_assertion description "[Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81109.RAirqHwucXOapo97g2iqkvyvSE8viNequ0LmTZeMj6Log130_provenance.
- NP81110.RAmcmP1sqmf_FWeHhDiw6jk4XZ9VQ6HOSvemFPa_6zFes130_assertion description "[Polymorphisms in the aurora-A gene is not associated with lung cancer in the Turkish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81110.RAmcmP1sqmf_FWeHhDiw6jk4XZ9VQ6HOSvemFPa_6zFes130_provenance.
- NP81113.RAkiSHmbkXBRSJqfzQUHLOyc2h4XqO1iUctU1K8QrnJt8130_assertion description "[Our results suggest that cell cycle gene polymorphisms and smoking may function collectively to modulate the risk of lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81113.RAkiSHmbkXBRSJqfzQUHLOyc2h4XqO1iUctU1K8QrnJt8130_provenance.
- NP81115.RAgysThoDWbjJUR49Xfot4qNOtw5nNkgtpdLSlwiP0PdM130_assertion description "[Genetic susceptibility to distinct bladder cancer subphenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81115.RAgysThoDWbjJUR49Xfot4qNOtw5nNkgtpdLSlwiP0PdM130_provenance.
- NP81117.RAsEw9FkNTHZKRTPmMn20QNXsvP_UDK9NZt_CiuUnGDhw130_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." NP81117.RAsEw9FkNTHZKRTPmMn20QNXsvP_UDK9NZt_CiuUnGDhw130_provenance.
- NP81118.RAoXLOCugfSg-kKhEZdEWvhQTakrKVce7z8KDd0vzJ7oI130_assertion description "[CyclinD1 and interleukin-1 receptor antagonist polymorphisms are associated with prognosis in neoadjuvant-treated gastric carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81118.RAoXLOCugfSg-kKhEZdEWvhQTakrKVce7z8KDd0vzJ7oI130_provenance.
- NP81121.RAsbJG-SwtxqMPE3IWVgteAbykdlqgqCdNSvLSwff-C5E130_assertion description "[Transcriptomic and genetic studies identify IL-33 as a candidate gene for Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81121.RAsbJG-SwtxqMPE3IWVgteAbykdlqgqCdNSvLSwff-C5E130_provenance.
- NP81133.RAikfQY350iUXn48c7Kkt2iMB13t7t2WEj7MrRPyQmbIw130_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." NP81133.RAikfQY350iUXn48c7Kkt2iMB13t7t2WEj7MrRPyQmbIw130_provenance.
- NP81141.RAtPy5yWBCN5X6x14AILnokjPII8X01MrTUzHoo_HSyQM130_assertion description "[The contribution of STAT4 for the genetic background of SLE may be greater in the Japanese population than in Americans of European descent.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81141.RAtPy5yWBCN5X6x14AILnokjPII8X01MrTUzHoo_HSyQM130_provenance.
- NP81151.RAjwk8LgwT0H_YrJ76KZiVM5Jn44eMn3HMsUGWjd-rR6w130_assertion description "[A regulatory variant in CCR6 is associated with rheumatoid arthritis susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81151.RAjwk8LgwT0H_YrJ76KZiVM5Jn44eMn3HMsUGWjd-rR6w130_provenance.
- NP81156.RAkcT0K-6oSMEImtGcgd9vNTxQ-YuDUNVNnVEAq7xLTng130_assertion description "[To test the hypothesis that the variant haplotype of STAT4 seen in RA and SLE is also associated with pSS, we genotyped rs7574865, the most strongly disease-associated SNP in the variant STAT4 haplotype, in 124 Caucasian pSS subjects and compared them to 1143 Caucasian controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81156.RAkcT0K-6oSMEImtGcgd9vNTxQ-YuDUNVNnVEAq7xLTng130_provenance.
- NP81160.RAslTx5wD2k_J62iGZh6cdbL83xxxRzEOj3Y1swSZD9_Q130_assertion description "[In an analysis of 1,039 SSc patients and 3,322 controls, the A allele of the STAT4 variant rs11889341 was associated with increased SSc susceptibility in a dominant pattern (Pcorr=2.4x10(-5), odds ratio 1.29, 95% confidence interval 1.2-1.5).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81160.RAslTx5wD2k_J62iGZh6cdbL83xxxRzEOj3Y1swSZD9_Q130_provenance.
- NP81166.RAmZ9JzTowWkbhIEmVXZYxm4Nsu278qFY-xPMeiIG0jm0130_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." NP81166.RAmZ9JzTowWkbhIEmVXZYxm4Nsu278qFY-xPMeiIG0jm0130_provenance.
- NP81170.RAkkxQTL9TPWdwScv-RAVNOqKx9gC5nnPxobbzrFeMqTY130_assertion description "[This study supports an underlying polygenic response to interferon beta treatment in MS and highlights the importance of the glutamatergic system in patient response to interferon beta therapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81170.RAkkxQTL9TPWdwScv-RAVNOqKx9gC5nnPxobbzrFeMqTY130_provenance.
- NP81173.RAumLyzeyjXADoaktgr82wpC0imihP556kwkVrocWfZhI130_assertion description "[We confirmed the association of multiple loci with UC in the Dutch population and found evidence for association of 10q26 and a trend suggesting association for GAS7.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81173.RAumLyzeyjXADoaktgr82wpC0imihP556kwkVrocWfZhI130_provenance.
- NP81188.RAkCy9kg1D5A9fFWh7fCsVhyQApjcUNrl32LVwesjFJiY130_assertion description "[Transcriptomic and genetic studies identify IL-33 as a candidate gene for Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81188.RAkCy9kg1D5A9fFWh7fCsVhyQApjcUNrl32LVwesjFJiY130_provenance.
- NP81192.RAuY2AuBhwMqGBoPOzDv-oEWFkVipcXlulXMzhQt_srm4130_assertion description "[Our results suggest that genetic variation in the SSTR5 gene and, particularly, the rs4988483 single nucleotide polymorphism influence circulating IGFI and IGFBP3 hormone levels with no measurable effect on prostate cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81192.RAuY2AuBhwMqGBoPOzDv-oEWFkVipcXlulXMzhQt_srm4130_provenance.
- NP81194.RAvO_QYhLLXMNArfu1flzLyWCtUmqMGod9Rku0fJxgFXs130_assertion description "[Genetic susceptibility to distinct bladder cancer subphenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81194.RAvO_QYhLLXMNArfu1flzLyWCtUmqMGod9Rku0fJxgFXs130_provenance.
- NP81213.RAurd6WO5ELlnf_DEwNEyH_igOB6zAAco6xv9_hb1Lx1Q130_assertion description "[Genetic variation in genes of the fatty acid synthesis pathway and breast cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81213.RAurd6WO5ELlnf_DEwNEyH_igOB6zAAco6xv9_hb1Lx1Q130_provenance.
- NP81221.RAruYNe9v8fJ4jKtSMzxOvKNJXBJaZeVCdyQh7iES7zps130_assertion description "[Polymorphism in the IL18 gene and epithelial ovarian cancer in non-Hispanic white women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81221.RAruYNe9v8fJ4jKtSMzxOvKNJXBJaZeVCdyQh7iES7zps130_provenance.
- NP81222.RAuxi6xzbv8GeaJDtZHG3MPDRnG1hvTI6Es18e1ZWqppg130_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." NP81222.RAuxi6xzbv8GeaJDtZHG3MPDRnG1hvTI6Es18e1ZWqppg130_provenance.
- NP81227.RAqkyPTI-KGZCihMSE2sYyj8rw-bHpWGM97nqtFxGTFYg130_assertion description "[Genetic variation of genes involved in dihydrotestosterone metabolism and the risk of prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81227.RAqkyPTI-KGZCihMSE2sYyj8rw-bHpWGM97nqtFxGTFYg130_provenance.
- NP81228.RAvHwW-HjQ7yd8pwuk1F6OH1ATxQ_o99ZtwZGJPfTzukg130_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." NP81228.RAvHwW-HjQ7yd8pwuk1F6OH1ATxQ_o99ZtwZGJPfTzukg130_provenance.
- NP81229.RAu2bAfU5MBnlaMBUNfzQOhWECxWc-spI_sIBHgiAKc6Q130_assertion description "[Genetic susceptibility to distinct bladder cancer subphenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81229.RAu2bAfU5MBnlaMBUNfzQOhWECxWc-spI_sIBHgiAKc6Q130_provenance.
- NP81235.RAkR11OIMH2pLSwTJtfeQ5MvdVs1c_Z1JR8U2nZUr6_js130_assertion description "[Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81235.RAkR11OIMH2pLSwTJtfeQ5MvdVs1c_Z1JR8U2nZUr6_js130_provenance.
- NP81237.RArVNsZ9VAoNmuXA8zCiua0J3XK6RuIqTXuZttz8ohRqM130_assertion description "[Examination of tetrahydrobiopterin pathway genes in autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81237.RArVNsZ9VAoNmuXA8zCiua0J3XK6RuIqTXuZttz8ohRqM130_provenance.
- NP81238.RAgWX2CM1Mf3C26B3hPj56KZs13M_1Syzn5hruTqoOfH0130_assertion description "[Exhaustive analysis of BH4 and dopamine biosynthesis genes in patients with Dopa-responsive dystonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81238.RAgWX2CM1Mf3C26B3hPj56KZs13M_1Syzn5hruTqoOfH0130_provenance.
- NP81242.RAmoFOyFfzJLRFLozwlcQkaRS1CZAAwsMzsi9TGEmhL30130_assertion description "[Patients with pancreas divisum presenting with idiopathic pancreatitis had a higher frequency of SPINK1 gene mutation compared with healthy controls, which might be responsible as the sole-factor or a co-factor in causing pancreatitis in them.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81242.RAmoFOyFfzJLRFLozwlcQkaRS1CZAAwsMzsi9TGEmhL30130_provenance.
- NP81248.RAvfkkVkWzgXOOv7sJhPwXzErWzYmOK89pGTV-SfwD7gM130_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." NP81248.RAvfkkVkWzgXOOv7sJhPwXzErWzYmOK89pGTV-SfwD7gM130_provenance.
- NP81260.RAloWdCYy3vNoOgpnXxoq7QDOZgjKCn0k5GmAxeGbbS9Q130_assertion description "[Genetic profiling of genes from the oxidative stress pathway among North and South Indians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81260.RAloWdCYy3vNoOgpnXxoq7QDOZgjKCn0k5GmAxeGbbS9Q130_provenance.
- NP81263.RAqJ_dRXdg4itoo5tQJ5JwEr5PB0wsjJ_3dsJLDzhcbxY130_assertion description "[When numeric scores were assigned to both the SNP and demographic data, and sequentially combined by a simple algorithm in a risk model, the composite score was found to be linearly related to lung cancer risk with a bimodal distribution.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81263.RAqJ_dRXdg4itoo5tQJ5JwEr5PB0wsjJ_3dsJLDzhcbxY130_provenance.