Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP79184.RAsntIPxWCt_F8DCKhlfsrZZs6dNh9aG42jlyZBeBOPxU130_assertion description "[Prostaglandin synthase 2/cyclooxygenase 2 (PTGS2/COX2) 8473T>C polymorphism associated with prognosis for patients with colorectal cancer treated with capecitabine and oxaliplatin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79184.RAsntIPxWCt_F8DCKhlfsrZZs6dNh9aG42jlyZBeBOPxU130_provenance.
- NP79187.RAipLTY9hDKUpzJML692d7pzYmZfqLqjf0ovMb_3M1Ezw130_assertion description "[These results suggest that a combined analysis of these three CASP gene polymorphisms might better predict the risk of lung cancer than analysis of a single polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79187.RAipLTY9hDKUpzJML692d7pzYmZfqLqjf0ovMb_3M1Ezw130_provenance.
- NP79189.RAp02Hqmp30Q__vvNASQqGHDJgpemEP0NSGfXeBxTyxEw130_assertion description "[the gastrointestinal stromal tumor tissues harbored a CASP mutation in 18.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79189.RAp02Hqmp30Q__vvNASQqGHDJgpemEP0NSGfXeBxTyxEw130_provenance.
- NP79190.RArTKDegPRmCryl_NO8N1l_xqLZaYTrSbeRo82aQnPnn4130_assertion description "[Genetic polymorphisms, their allele combinations and IFN-beta treatment response in Irish multiple sclerosis patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79190.RArTKDegPRmCryl_NO8N1l_xqLZaYTrSbeRo82aQnPnn4130_provenance.
- NP79193.RAnNjIYmI5mfDLwX2HU5IHJ2zX1vNpGjBu6XmrZaorC9A130_assertion description "[the gastrointestinal stromal tumor tissues harbored a CASP mutation in 18.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79193.RAnNjIYmI5mfDLwX2HU5IHJ2zX1vNpGjBu6XmrZaorC9A130_provenance.
- NP79194.RAn1qzUBRnwjl_UNb_Xtp-8gvYuSswD7dH2c42f43V-Cg130_assertion description "[the gastrointestinal stromal tumor tissues harbored a CASP mutation in 18.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79194.RAn1qzUBRnwjl_UNb_Xtp-8gvYuSswD7dH2c42f43V-Cg130_provenance.
- NP79196.RAtOq24zFISpaCKPQIwzUlqwrwcSTBtukff4qSXRjXrOE130_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." NP79196.RAtOq24zFISpaCKPQIwzUlqwrwcSTBtukff4qSXRjXrOE130_provenance.
- NP79200.RAlkgjveqCxAj6hG41qGDkREEEdJmaSKZpX03u3snbTbI130_assertion description "[Our data indicate that somatic mutation of the CASP4 gene is common in gastrointestinal stromal tumor and suggest a possibility that CASP4 mutation might lead to alteration of apoptotic or inflammatory function and contribute to the pathogenesis of some gastrointestinal stromal tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79200.RAlkgjveqCxAj6hG41qGDkREEEdJmaSKZpX03u3snbTbI130_provenance.
- NP79201.RArDVfDvZ1tR9o9xNrYNGQfZbx1zpQMuE5YVQz7AaTjYU130_assertion description "[Genetic polymorphisms, their allele combinations and IFN-beta treatment response in Irish multiple sclerosis patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79201.RArDVfDvZ1tR9o9xNrYNGQfZbx1zpQMuE5YVQz7AaTjYU130_provenance.
- NP79204.RAjxIqgRg7yfjsGbDAuPYS9EUA9aoqOTeR5JpGesjhaUw130_assertion description "[Polymorphisms in the CASPASE genes and survival in patients with early-stage non-small-cell lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79204.RAjxIqgRg7yfjsGbDAuPYS9EUA9aoqOTeR5JpGesjhaUw130_provenance.
- NP79214.RAj0RQy81pbrwK_sQDCvP-Bc-Xfvdatu-ocAhIHlEMqac130_assertion description "[the gastrointestinal stromal tumor tissues harbored a CASP mutation in 18.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79214.RAj0RQy81pbrwK_sQDCvP-Bc-Xfvdatu-ocAhIHlEMqac130_provenance.
- NP79218.RAnxH_AHfNpC5DMi0TMWtHm4QZsNHi59EsZPvOppS4R4Y130_assertion description "[the gastrointestinal stromal tumor tissues harbored a CASP mutation in 18.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79218.RAnxH_AHfNpC5DMi0TMWtHm4QZsNHi59EsZPvOppS4R4Y130_provenance.
- NP79220.RAhPt4UVsb-Tnap5z6Lru5VD79fQbfGH7N03AbrT8uvuQ130_assertion description "[We found association with CLL susceptibility and 22 haplotypes in APAF1, IL6, TNFRSF13B, IL16, CASP3, CCR7, LTA/TNF, BAX, BCL2, CXCL12, CASP10/CASP8, CASP1, CCL2, BAK1, and IL1A candidate genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79220.RAhPt4UVsb-Tnap5z6Lru5VD79fQbfGH7N03AbrT8uvuQ130_provenance.
- NP79224.RAnrSpYInNAJ4eYHVWSMPsfn26wzB-_xMeZJC9CfLNBM8130_assertion description "[the gastrointestinal stromal tumor tissues harbored a CASP mutation in 18.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79224.RAnrSpYInNAJ4eYHVWSMPsfn26wzB-_xMeZJC9CfLNBM8130_provenance.
- NP79227.RAjPKnRANEzxgPIfCzSh2eaEMuMt2_GLyZCX3l9uMRsZY130_assertion description "[Genetic polymorphisms, their allele combinations and IFN-beta treatment response in Irish multiple sclerosis patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79227.RAjPKnRANEzxgPIfCzSh2eaEMuMt2_GLyZCX3l9uMRsZY130_provenance.
- NP79240.RAovYInF_hZa5ATbYI_VmXCHmWWZEEZ2O7paVTCzfHKKk130_assertion description "[A genome-wide association study identifies novel and functionally related susceptibility Loci for Kawasaki disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79240.RAovYInF_hZa5ATbYI_VmXCHmWWZEEZ2O7paVTCzfHKKk130_provenance.
- NP79242.RAmBixdN3nrfnsCWgqOR3YLeq-aQL1uUAEdZADakKwRhg130_assertion description "[Association of SIRT1 gene variation with visceral obesity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79242.RAmBixdN3nrfnsCWgqOR3YLeq-aQL1uUAEdZADakKwRhg130_provenance.
- NP79244.RAnOoUXfI69GzCjNYyRZfb1KAGEiZyyQ2gU9D02HsP2g0130_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." NP79244.RAnOoUXfI69GzCjNYyRZfb1KAGEiZyyQ2gU9D02HsP2g0130_provenance.
- NP79259.RApFyvvsmLw2Igj_I8EC-qCnoiUR_-Y0CiqQpkjYZNI3w130_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." NP79259.RApFyvvsmLw2Igj_I8EC-qCnoiUR_-Y0CiqQpkjYZNI3w130_provenance.
- NP79260.RAohhdZt-IE8s1wD6apft-Ob8PjLcGm1Ry8Rz3C5WztlE130_assertion description "[Interaction between Calpain 5, Peroxisome proliferator-activated receptor-gamma and Peroxisome proliferator-activated receptor-delta genes: a polygenic approach to obesity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79260.RAohhdZt-IE8s1wD6apft-Ob8PjLcGm1Ry8Rz3C5WztlE130_provenance.
- NP79278.RAikUonuxeZkESLkEpo55JyJsq_ycjFzORj4SQn1b5icw130_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." NP79278.RAikUonuxeZkESLkEpo55JyJsq_ycjFzORj4SQn1b5icw130_provenance.
- NP79279.RAl8vd1qMfKAht_0q2uI4ZS4swuE6ukI_ytGZF6Ndi95g130_assertion description "[Genetic variations in NR2A have the greatest relevance for human alcohol dependence among the glutamatergic genes selected for their known alteration of alcohol effects in animal models.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79279.RAl8vd1qMfKAht_0q2uI4ZS4swuE6ukI_ytGZF6Ndi95g130_provenance.
- NP79280.RAu0a0kwsf3FY0NJHm5FH2HEgx9m-haVfE_sIfMGHVWFg130_assertion description "[These results support polygenic genetics for success in abstaining from smoking, overlap with genetics of substance dependence and memory, and nominate gene variants for selective influences on therapeutic responses to bupropion vs NRT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79280.RAu0a0kwsf3FY0NJHm5FH2HEgx9m-haVfE_sIfMGHVWFg130_provenance.
- NP79283.RAr0VuNRm359DOpVgEA8NSggyyiHSbK4QR0Nt3biRQskM130_assertion description "[A genome-wide association study identifies novel and functionally related susceptibility Loci for Kawasaki disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79283.RAr0VuNRm359DOpVgEA8NSggyyiHSbK4QR0Nt3biRQskM130_provenance.
- NP79284.RAmj9iiTlK9EDfajNIYIzabKw8BM9Iyn1QGqWeFOEiuEI130_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." NP79284.RAmj9iiTlK9EDfajNIYIzabKw8BM9Iyn1QGqWeFOEiuEI130_provenance.
- NP79285.RAg52DeLsBe3ImudjCpE6jblvEyDd_lqTj33_DkPuGcCQ130_assertion description "[High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79285.RAg52DeLsBe3ImudjCpE6jblvEyDd_lqTj33_DkPuGcCQ130_provenance.
- NP79289.RAjYlEhgPWv3K1flu0R4skXDJfQRMFo3qoSIUCm0vxe5M130_assertion description "[Family-based association study for bipolar affective disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79289.RAjYlEhgPWv3K1flu0R4skXDJfQRMFo3qoSIUCm0vxe5M130_provenance.
- NP79297.RAnxQF-vJtc2vhRV9hknA3BYgecaTYbKSgeFAvcH69Ssc130_assertion description "[Association of polymorphisms of SORBS1, GCK and WISP1 with hypertension in community-dwelling Japanese individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79297.RAnxQF-vJtc2vhRV9hknA3BYgecaTYbKSgeFAvcH69Ssc130_provenance.
- NP79304.RAnK3sGIa5WzUZepg6ciNPONP5eQIn3cDXe78OlYU0nFA130_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." NP79304.RAnK3sGIa5WzUZepg6ciNPONP5eQIn3cDXe78OlYU0nFA130_provenance.
- NP79309.RAm_pqkHj_-5osGCvLQk4GgWQNgaLeo_xA7j_Uzv4NNhE130_assertion description "[Genetic susceptibility factors in a cohort of 38 patients with SAPHO syndrome: a study of PSTPIP2, NOD2, and LPIN2 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79309.RAm_pqkHj_-5osGCvLQk4GgWQNgaLeo_xA7j_Uzv4NNhE130_provenance.
- NP79312.RAvWy0ym3trrFM3ehF8jSneBTTc166H0kfpUs5nc6Eb4g130_assertion description "[Genetic susceptibility to distinct bladder cancer subphenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79312.RAvWy0ym3trrFM3ehF8jSneBTTc166H0kfpUs5nc6Eb4g130_provenance.
- NP79314.RAkwjaaK2DPO2JVU6_xSOed6tjl4C5ws4W-wZvfEfPDo0130_assertion description "[Is calmodulin 1 gene/estrogen receptor-alpha gene polymorphisms correlated with double curve pattern of adolescent idiopathic scoliosis?.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79314.RAkwjaaK2DPO2JVU6_xSOed6tjl4C5ws4W-wZvfEfPDo0130_provenance.
- NP79316.RAki4ET5kG1j1ICGrBfheJ4a6EJN4auHZ6O1RT7QlaFf4130_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." NP79316.RAki4ET5kG1j1ICGrBfheJ4a6EJN4auHZ6O1RT7QlaFf4130_provenance.
- NP79319.RAl2Ua8HiGDPOnHg_rbVNTfz0dYjkNOcGcUcbROuEvAWM130_assertion description "[Genetic and environmental factors in human osteoporosis from Sub-Saharan to Mediterranean areas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79319.RAl2Ua8HiGDPOnHg_rbVNTfz0dYjkNOcGcUcbROuEvAWM130_provenance.
- NP79321.RAgTb4Nux6OPCDU1uj1uuYp4pLWjr0N9dGEWXDuPb7CyA130_assertion description "[Identification of novel genetic susceptibility loci for Behet's disease using a genome-wide association study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79321.RAgTb4Nux6OPCDU1uj1uuYp4pLWjr0N9dGEWXDuPb7CyA130_provenance.
- NP79329.RApZi_DqxObqSL66OhCWfw6pkTiuc4XFRrMoM_VotyveY130_assertion description "[A novel autosomal dominant high myopia locus was mapped on chromosome 5p15.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79329.RApZi_DqxObqSL66OhCWfw6pkTiuc4XFRrMoM_VotyveY130_provenance.
- NP79333.RAvSzqCmLcRUbwBVz-foa8AdP1_S9eKDPq8zY6B0VSJDA130_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." NP79333.RAvSzqCmLcRUbwBVz-foa8AdP1_S9eKDPq8zY6B0VSJDA130_provenance.
- NP79340.RAnJVkLw5yA9-NwtgtyKglx7Y3BVDVYRiOINOx19ajkFo130_assertion description "[Association between the SERPING1 gene and age-related macular degeneration: a two-stage case-control study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79340.RAnJVkLw5yA9-NwtgtyKglx7Y3BVDVYRiOINOx19ajkFo130_provenance.
- NP79347.RAsIsTe-UIYQFHj0ubgnonO0AgA0HykeWtWYHO1am5e9w130_assertion description "[Recently, mutations in two X-linked neuroligin genes, neuroligin 3 (NLGN3) and neuroligin 4 (NLGN4), have been implicated in the pathogenesis of autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79347.RAsIsTe-UIYQFHj0ubgnonO0AgA0HykeWtWYHO1am5e9w130_provenance.
- NP79361.RAvZLLAkC98CBgd2yGMzDk0qgEgxip5pnQkPS3NLjPOz8130_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." NP79361.RAvZLLAkC98CBgd2yGMzDk0qgEgxip5pnQkPS3NLjPOz8130_provenance.
- NP79369.RAgPYe2BD1qB0gHPuUe8hr3W1ZzYpHuw1FUDWj-2c7K5Y130_assertion description "[Genetic variants identified in a European genome-wide association study that were found to predict incident coronary heart disease in the atherosclerosis risk in communities study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79369.RAgPYe2BD1qB0gHPuUe8hr3W1ZzYpHuw1FUDWj-2c7K5Y130_provenance.
- NP79380.RApfkOYVSbC5GaY0Kja6_nWz5xE8rnC74U2rmEaoNoOZA130_assertion description "[The genes RASD2, MYH9, and CACNG2 might be vulnerability genes for neuropsychologically defined subgroups of schizophrenic patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79380.RApfkOYVSbC5GaY0Kja6_nWz5xE8rnC74U2rmEaoNoOZA130_provenance.
- NP79381.RAmEOwSg_y-tINzrBGmlz18GVc_vXf3UM4G9kvXFU2Yao130_assertion description "[Our findings suggest that Stargazin dysregulation may be involved with the pathophysiology of BPD, but not with that of schizophrenia, and that Stargazin polymorphisms may play a role in the response to lithium treatment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79381.RAmEOwSg_y-tINzrBGmlz18GVc_vXf3UM4G9kvXFU2Yao130_provenance.
- NP79388.RAqIfJNfvqdPxkCOZ4WSBt_JE8Ajl0soNlijFTNdDZk3Y130_assertion description "[Prognostic relevance of DNA copy number changes in colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79388.RAqIfJNfvqdPxkCOZ4WSBt_JE8Ajl0soNlijFTNdDZk3Y130_provenance.
- NP79390.RAsE7zoROkHym5hG3BcfKttpQDMtYY7Je96plKolHmxy4130_assertion description "[We have confirmed 7 loci associated with blood pressure and/or hypertension in the Japanese. These loci can guide fine-mapping efforts to pinpoint causal variants and causal genes with the integration of multiethnic results.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79390.RAsE7zoROkHym5hG3BcfKttpQDMtYY7Je96plKolHmxy4130_provenance.
- NP79397.RAvoFwF6DMLIv7EHw0Hw6wSd_srrmdDinrv9Dvgm5NMEw130_assertion description "[Common variants on chromosome 6p22.1 are associated with schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79397.RAvoFwF6DMLIv7EHw0Hw6wSd_srrmdDinrv9Dvgm5NMEw130_provenance.
- NP79401.RAguQFE35GB2kKVLAVWwJoV8Be8-kyIMnISbjPqmq6xeU130_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." NP79401.RAguQFE35GB2kKVLAVWwJoV8Be8-kyIMnISbjPqmq6xeU130_provenance.
- NP79404.RAvPk2gsLE7zUA54EckorXQiuVFGK2rxVeUKR5TypXy4s130_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." NP79404.RAvPk2gsLE7zUA54EckorXQiuVFGK2rxVeUKR5TypXy4s130_provenance.
- NP79411.RAh_w8vk8nq-LA_eFX2daDIt0ldcDWzz6lSMdOvszxJY4130_assertion description "[Contribution of a haplotype in the HLA region to anti-cyclic citrullinated peptide antibody positivity in rheumatoid arthritis, independently of HLA-DRB1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79411.RAh_w8vk8nq-LA_eFX2daDIt0ldcDWzz6lSMdOvszxJY4130_provenance.
- NP79415.RAgciFiQy6kqaXxvf_T_77kuHqy6ALJr8g7AMutfPDZD8130_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." NP79415.RAgciFiQy6kqaXxvf_T_77kuHqy6ALJr8g7AMutfPDZD8130_provenance.
- NP79417.RAtiDBAA1tKtwhGU30VS56EcNyJ4xivjopL-X730ySfEY130_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." NP79417.RAtiDBAA1tKtwhGU30VS56EcNyJ4xivjopL-X730ySfEY130_provenance.
- NP79420.RAj6TWURAp95YKgubcXIM_W82xzd_AAjMCXgjjQjlPISw130_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." NP79420.RAj6TWURAp95YKgubcXIM_W82xzd_AAjMCXgjjQjlPISw130_provenance.
- NP79432.RAn8Q8IRSiFATudgYWsMv2qZI3qy7iII5slQa9wpmHH3U130_assertion description "[Multiple Loci within the major histocompatibility complex confer risk of psoriasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79432.RAn8Q8IRSiFATudgYWsMv2qZI3qy7iII5slQa9wpmHH3U130_provenance.
- NP79439.RAu10mvl1gyeXMKuXZKwvAUd3T9El_zoaEDvStprsxuBg130_assertion description "[Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79439.RAu10mvl1gyeXMKuXZKwvAUd3T9El_zoaEDvStprsxuBg130_provenance.
- NP79452.RAr--64KBfXr9UIIaDPIAcYZL5IoSKGeXRo3anka_-ViM130_assertion description "[Genetic variation in the pleiotropic psychiatric disease gene CACNA1C is associated with brainstem volume. Modulation of this structure, with its central control over motor, cognitive, affective, and arousal functions, constitutes an interesting novel potential mode of action of psychiatric risk factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79452.RAr--64KBfXr9UIIaDPIAcYZL5IoSKGeXRo3anka_-ViM130_provenance.
- NP79454.RAo_T1NUVeC_ikgTx9SmAR0wfUDAdWK6Uy2iS_U0prNSY130_assertion description "[Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79454.RAo_T1NUVeC_ikgTx9SmAR0wfUDAdWK6Uy2iS_U0prNSY130_provenance.
- NP79462.RAmHQBtmQM71JK_tlY9-bVc5NP2wEhdKj1BTqs0I2alUY130_assertion description "[The results suggest that the DH genotype and the H allele of the ABCG8 D19H polymorphism are associated with GBC susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79462.RAmHQBtmQM71JK_tlY9-bVc5NP2wEhdKj1BTqs0I2alUY130_provenance.
- NP79463.RAnqI7o2eCfRm6PjGiSnvD4E_yCSO4LKS5hbnXCy2lKm0130_assertion description "[Genetic susceptibility to distinct bladder cancer subphenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79463.RAnqI7o2eCfRm6PjGiSnvD4E_yCSO4LKS5hbnXCy2lKm0130_provenance.
- NP79464.RApEN1QYXvHSqTvqw8tzH7iw59Mf00etMBA9n3EQEcNBc130_assertion description "[ABCG5 and ABCG8 genes were not associated with the risk of CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79464.RApEN1QYXvHSqTvqw8tzH7iw59Mf00etMBA9n3EQEcNBc130_provenance.
- NP79466.RAqnlcXVMvMrH6xXN1TIjjwRFnLGv_8iFTF8yp8Ia-zJ4130_assertion description "[Carriers of ABCG5 604Q or ABCG8 D19H polymorphisms have an increased risk of gallstone disease independent of age, sex and body mass index.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79466.RAqnlcXVMvMrH6xXN1TIjjwRFnLGv_8iFTF8yp8Ia-zJ4130_provenance.
- NP79468.RAhkz-O2YNQ1Yy0UNqFiJ4qfTmfirvbGkhg909QIJCRAI130_assertion description "[Carriers of ABCG5 604Q or ABCG8 D19H polymorphisms have an increased risk of gallstone disease independent of age, sex and body mass index.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79468.RAhkz-O2YNQ1Yy0UNqFiJ4qfTmfirvbGkhg909QIJCRAI130_provenance.
- NP79471.RAk3w6qwLfQV90XO2qGlA9790CaClwB7Lwg_XO2Nkweds130_assertion description "[A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79471.RAk3w6qwLfQV90XO2qGlA9790CaClwB7Lwg_XO2Nkweds130_provenance.
- NP79476.RAgZrnw5uTzHR32VSELR8SoZswgII8hgzNpi1yPfy-xXU130_assertion description "[The interplay of two single nucleotide polymorphisms in the CACNA1A gene may contribute to migraine susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79476.RAgZrnw5uTzHR32VSELR8SoZswgII8hgzNpi1yPfy-xXU130_provenance.
- NP79481.RAt8rr10m65F8452p-DvEnUXP50Ftpl2hiAiQ1WzpvKG8130_assertion description "[Genome-wide association scan for five major dimensions of personality.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79481.RAt8rr10m65F8452p-DvEnUXP50Ftpl2hiAiQ1WzpvKG8130_provenance.
- NP79482.RAh7Yxhc94zAZxRglw7qpomOqMtUTf07UYGjy1lmu-nT8130_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." NP79482.RAh7Yxhc94zAZxRglw7qpomOqMtUTf07UYGjy1lmu-nT8130_provenance.
- NP79491.RAv3DXTYSzv4Ky1pAd5TNmowRtsgcRZVUQKemuF70q2-k130_assertion description "[Multiple cholinergic nicotinic receptor genes affect nicotine dependence risk in African and European Americans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79491.RAv3DXTYSzv4Ky1pAd5TNmowRtsgcRZVUQKemuF70q2-k130_provenance.
- NP79492.RAj9ldBXk7oGyPCKyZto7p2yN33w5_mLV8flw2diVBtT0130_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." NP79492.RAj9ldBXk7oGyPCKyZto7p2yN33w5_mLV8flw2diVBtT0130_provenance.
- NP79497.RAr8PB9ViMgpEqJFIHb7MXlbIBsHg4EriUlEeVfp0iJqk130_assertion description "[For ADAM33, NPSR1, and CYFIP2, the associations with asthma or asthma-related phenotypes have been studied in East Asian populations such as Chinese and Japanese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79497.RAr8PB9ViMgpEqJFIHb7MXlbIBsHg4EriUlEeVfp0iJqk130_provenance.
- NP79505.RAgNbb42pqo3c7W6kx9Le11xs9nl4ltAp4wyIS5Z2-H7g130_assertion description "[Here, we investigated single nucleotide polymorphisms (SNPs) in carbonic anhydrase genes that are expressed in bone tissues, i.e., CA8 and CA10, for possible association with femoral and lumbar BMD among 337 Japanese women with osteoporosis participated in BioBank Japan project.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79505.RAgNbb42pqo3c7W6kx9Le11xs9nl4ltAp4wyIS5Z2-H7g130_provenance.
- NP79509.RAhcxXVMSNNkyygZhb6_GF1hYLcoTvuZtjMwt0Jm-dZoY130_assertion description "[Association of the +45T>G and +276G>T polymorphisms in the adiponectin gene with insulin resistance in nondiabetic Greek women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79509.RAhcxXVMSNNkyygZhb6_GF1hYLcoTvuZtjMwt0Jm-dZoY130_provenance.
- NP79512.RAtNQsSs6s-pNWzJ5a9i5zaL4qm4UximnYonY8aZOINOk130_assertion description "[Adiponectin gene polymorphisms are associated with long-chain 3-polyunsaturated fatty acids in serum phospholipids in nondiabetic Koreans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79512.RAtNQsSs6s-pNWzJ5a9i5zaL4qm4UximnYonY8aZOINOk130_provenance.
- NP79514.RAs_0Wsk_vgDUUQC86oNnEVHLvlinYuDashzp3Vcjxf5c130_assertion description "[A recent study examined common genetic variants at the adiponectin locus (ADIPOQ) in two case-control colorectal cancer (CRC) series from the USA and reported a positive association between a single nucleotide polymorphism (SNP) in the 5' region of the gene (rs266729) and decreased disease risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79514.RAs_0Wsk_vgDUUQC86oNnEVHLvlinYuDashzp3Vcjxf5c130_provenance.
- NP79515.RAqu2tPxN40j7muIFbflSSOIgIlJHxFcipucw0FHwtzxw130_assertion description "[We hypothesized that potentially functional polymorphisms in the adipokine genes leptin (LEP), leptin receptor (LEPR), resistin (RETN), and adiponectin (ADIPOQ) may be associated with CRC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79515.RAqu2tPxN40j7muIFbflSSOIgIlJHxFcipucw0FHwtzxw130_provenance.
- NP79516.RAoAr2PiocJpsSfhC8tVGsK4khHNl4GJTzQo_EGO4PQ94130_assertion description "[Our study suggests that polymorphisms in IL10, and also possibly in CRP and other genes related to immune response or obesity may be associated with colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79516.RAoAr2PiocJpsSfhC8tVGsK4khHNl4GJTzQo_EGO4PQ94130_provenance.
- NP79518.RAusEVvxmJCejVRDUvRnmZ1OzQilNw8q4kAqPoTWlV_zY130_assertion description "[Our prospective study suggests that genetic variation in IL10 and possibly TLR4 is associated with prostate cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79518.RAusEVvxmJCejVRDUvRnmZ1OzQilNw8q4kAqPoTWlV_zY130_provenance.
- NP79519.RAo0dwGRANR3ESxz8qa5ibEKpoiBC0W100ZKkSpq-AujU130_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." NP79519.RAo0dwGRANR3ESxz8qa5ibEKpoiBC0W100ZKkSpq-AujU130_provenance.
- NP79522.RAstocQVBxZ3KqJXnzvnixl7AhkmrI2BCAMkVIS89TAWY130_assertion description "[Severe obesity in Han Chinese was associated with 3 novel common SNPs for ESR1 and PPARgamma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79522.RAstocQVBxZ3KqJXnzvnixl7AhkmrI2BCAMkVIS89TAWY130_provenance.
- NP79524.RAvaJhWXGQl8ZW94yYWinCNOiJIdgqyMEjARS6q1nTq_Y130_assertion description "[FBXL21 association with schizophrenia in Irish family and case-control samples.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79524.RAvaJhWXGQl8ZW94yYWinCNOiJIdgqyMEjARS6q1nTq_Y130_provenance.
- NP79530.RAuJ6crrDErCot3iJSf3WridWoVdIqD6SaUgWi-oU0TN0130_assertion description "[Angiotensin-converting enzyme 2 A1075G polymorphism is associated with survival in an acute coronary syndromes cohort.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79530.RAuJ6crrDErCot3iJSf3WridWoVdIqD6SaUgWi-oU0TN0130_provenance.
- NP79531.RApZmMEHZdExFeA5lBsFtml9RDpPoGYkFNzBBJlZofbj4130_assertion description "[Our genomewide association analysis again identified the APOE linkage disequilibrium region as the strongest genetic risk factor for AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79531.RApZmMEHZdExFeA5lBsFtml9RDpPoGYkFNzBBJlZofbj4130_provenance.
- NP79536.RAi40y5MyCZo4D2YUtLc8eqzSnLAKiuWlGXVMWbQgHtn8130_assertion description "[These results support polygenic genetics for success in abstaining from smoking, overlap with genetics of substance dependence and memory, and nominate gene variants for selective influences on therapeutic responses to bupropion vs NRT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79536.RAi40y5MyCZo4D2YUtLc8eqzSnLAKiuWlGXVMWbQgHtn8130_provenance.
- NP79537.RAqEUILh1vbjVRRBO1BBLjTijuLWvzjx-qhgjCF3LJeXQ130_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." NP79537.RAqEUILh1vbjVRRBO1BBLjTijuLWvzjx-qhgjCF3LJeXQ130_provenance.
- NP79540.RAluopVQMfVz2g7uUiGissGoGjPKm7Cfr6-dOqJyZSlNs130_assertion description "[DC-SIGNR polymorphisms and its association with HIV-1 infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79540.RAluopVQMfVz2g7uUiGissGoGjPKm7Cfr6-dOqJyZSlNs130_provenance.
- NP79550.RAgtLPEvaN7Zf7sx9u5A9Bl8DQqIZNaNv3re2yyjpr9DI130_assertion description "[Use of a genetic isolate to identify rare disease variants: C7 on 5p associated with MS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79550.RAgtLPEvaN7Zf7sx9u5A9Bl8DQqIZNaNv3re2yyjpr9DI130_provenance.
- NP79554.RAuy91wlsu8PoW-XNHx9wof6jpb6EaMuPnA8SnDc8fVzM130_assertion description "[SNP markers in SLC2A9 and ABCG2 genes were found to be strongly associated with the phenotype gout.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79554.RAuy91wlsu8PoW-XNHx9wof6jpb6EaMuPnA8SnDc8fVzM130_provenance.
- NP79556.RAq0ihF2hvWeMuUE_AHaQkGknhz8VElQS46wleBk76dFs130_assertion description "[We also investigated whether we could provide support for three regions previously associated with BD, and we showed that the ANK3 region replicates in our sample, along with some support for C15Orf53; other evidence implicates BD candidate genes such as SLITRK2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79556.RAq0ihF2hvWeMuUE_AHaQkGknhz8VElQS46wleBk76dFs130_provenance.
- NP79557.RArDOV4O1SWHbj-SYm3W6DnLF_Lds6vKSv4a3bH7u6iUw130_assertion description "[Our results suggest that there are multiple genetic variants within or near hURAT1 that are associated with susceptibility to HUA in Han Chinese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79557.RArDOV4O1SWHbj-SYm3W6DnLF_Lds6vKSv4a3bH7u6iUw130_provenance.
- NP79558.RAt_IZh68s5UxxqJe1nBkcdd2GwbYKKNcTn0SirVi3ANI130_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." NP79558.RAt_IZh68s5UxxqJe1nBkcdd2GwbYKKNcTn0SirVi3ANI130_provenance.
- NP79563.RAgUPQmWT2U9IthhJZwHDQTIdN029KDsgyFeZm7uVKwe0130_assertion description "[A prior genome-wide association (GWA) study in Pima Indians identified variants within PCLO that were associated with early-onset type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79563.RAgUPQmWT2U9IthhJZwHDQTIdN029KDsgyFeZm7uVKwe0130_provenance.
- NP79567.RAi7S_9Y7Pf6s8kONkcB1QdwV2T-u-kOBcQzgcxD9USTI130_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." NP79567.RAi7S_9Y7Pf6s8kONkcB1QdwV2T-u-kOBcQzgcxD9USTI130_provenance.
- NP79569.RAjTAMUuS0RIN38wNCbySelFrBPu4WvRRPkomzDh2ajIc130_assertion description "[Association between the SERPING1 gene and age-related macular degeneration: a two-stage case-control study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79569.RAjTAMUuS0RIN38wNCbySelFrBPu4WvRRPkomzDh2ajIc130_provenance.
- NP79575.RAva6GZzzVZkKWHnQMIVuQ5GGdoFeHEhV35igTjS4joig130_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." NP79575.RAva6GZzzVZkKWHnQMIVuQ5GGdoFeHEhV35igTjS4joig130_provenance.
- NP79583.RAjlpujvwidbY6wE1V1ULyicu-qdKBi1ji2RyZo0S6IMs130_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." NP79583.RAjlpujvwidbY6wE1V1ULyicu-qdKBi1ji2RyZo0S6IMs130_provenance.
- NP79585.RAq0NCM5lSt4eH_DlD9W82uTLe3Z-8k4RzJTQv_oEMjVU130_assertion description "[TRAF1/C5 polymorphism is not associated with pemphigus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79585.RAq0NCM5lSt4eH_DlD9W82uTLe3Z-8k4RzJTQv_oEMjVU130_provenance.
- NP79586.RAkVAgLR9uUp19I2ENb8aFFJyNGBIhdcw9ymufx-B-8TI130_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." NP79586.RAkVAgLR9uUp19I2ENb8aFFJyNGBIhdcw9ymufx-B-8TI130_provenance.
- NP79590.RAh29p65FrIbLVbtOWGw5LZihyIlc6gwOU0Fl5QG0jkgA130_assertion description "[Although the complement pathway, including C5, plays a crucial role in AMD, and the C5 protein is present in drusen, no consistent significant associations between C5 SNPs and AMD were found in any of these studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79590.RAh29p65FrIbLVbtOWGw5LZihyIlc6gwOU0Fl5QG0jkgA130_provenance.
- NP79597.RAqCaAjn4aXRcLV1ROKwWdh8qCNPfQbjsCAE0kKy0Mt5k130_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." NP79597.RAqCaAjn4aXRcLV1ROKwWdh8qCNPfQbjsCAE0kKy0Mt5k130_provenance.
- NP79600.RAvkT1i6V-oqWyefaJFAubqSW9o4VcOtAUPZC2_JaT7Rs130_assertion description "[Genetic variations in FTSJ1 influence cognitive ability in young males in the Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79600.RAvkT1i6V-oqWyefaJFAubqSW9o4VcOtAUPZC2_JaT7Rs130_provenance.
- NP79602.RArFgnKltWIm6ksPsPuelYxO3V8vGHECPY62S2WBtw39Q130_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." NP79602.RArFgnKltWIm6ksPsPuelYxO3V8vGHECPY62S2WBtw39Q130_provenance.
- NP79605.RAnS0PuCeCgw7iWaK3JBcg1qjS7Jq1voqmQnoXhXSTA9k130_assertion description "[High-throughput analysis of the C4 polymorphism by a combination of MLPA and isotype-specific ELISA's.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79605.RAnS0PuCeCgw7iWaK3JBcg1qjS7Jq1voqmQnoXhXSTA9k130_provenance.