Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP43995.RAqYJGe5LPpSjMRkGmXyyIT1wwnrF8zwObkZMd28PkPXo130_assertion description "[Despite intensive investigation, there is no clear evidence for a role of variations in the genes coding for the fibrinogen-alpha, fibrinogen-beta, and fibrinogen-gamma polypeptide chains in myocardial infarction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43995.RAqYJGe5LPpSjMRkGmXyyIT1wwnrF8zwObkZMd28PkPXo130_provenance.
- NP43997.RAtZEYMroJlzoOXigfTplaxdfr9jOwsfFG6uACilVEFNY130_assertion description "[ This study is one of the first comprehensive mutational analyses of major genes in a specific signaling pathway in a sizeable cohort of lung adenocarcinomas. Our results suggest the majority of gain-of-function mutations within kinase genes in the EGFR signaling pathway have already been identified. Our findings also implicate FGFR4 in the pathogenesis of a subset of lung adenocarcinomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43997.RAtZEYMroJlzoOXigfTplaxdfr9jOwsfFG6uACilVEFNY130_provenance.
- NP43998.RAreU19lV62NASy6Dzne0tgggyjejuoYfaIxqnjbzzdl8130_assertion description "[Further observations on the relationship between the FGFR4 Gly388Arg polymorphism and lung cancer prognosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43998.RAreU19lV62NASy6Dzne0tgggyjejuoYfaIxqnjbzzdl8130_provenance.
- NP43999.RAmmw0LPbtGIoKRkxxHO7eyiqywIDEdKJE7i6Gk1yGvBs130_assertion description "[Fibroblast growth factor receptor 4 mutation and polymorphism in Japanese lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43999.RAmmw0LPbtGIoKRkxxHO7eyiqywIDEdKJE7i6Gk1yGvBs130_provenance.
- NP44002.RAsrLzX4Bkv_9mhZzm3mRaFYkHUgGT5xqbl7Rixwf5mNQ130_assertion description "[Polymorphism of FGFR4 Gly388Arg does not confer an increased risk to breast cancer development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44002.RAsrLzX4Bkv_9mhZzm3mRaFYkHUgGT5xqbl7Rixwf5mNQ130_provenance.
- NP44005.RAsfgaDNlSQvWrbJRsndqrAKDs1y8F2oz4SEJb_zS-Yc8130_assertion description "[Polymorphisms of fibroblast growth factor receptor 4 have association with the development of prostate cancer and benign prostatic hyperplasia and the progression of prostate cancer in a Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44005.RAsfgaDNlSQvWrbJRsndqrAKDs1y8F2oz4SEJb_zS-Yc8130_provenance.
- NP44006.RAvRrm9CO-giKjeleMMRd4DY3V_tfwO8KFksOTjNFuzaI130_assertion description "[Association of FGFR4 genetic polymorphisms with prostate cancer risk and prognosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44006.RAvRrm9CO-giKjeleMMRd4DY3V_tfwO8KFksOTjNFuzaI130_provenance.
- NP44007.RAlvUR4aC9j-q7RR4CfYs_jlyLNYs04ah4NAQ3ZwJeK7A130_assertion description "[A single nucleotide polymorphism at position 388 of the FGFR4 amino-acid sequence results in the substitution of glycine (Gly) with arginine (Arg) and higher frequency of the ArgArg genotype was previously found in prostate cancer patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44007.RAlvUR4aC9j-q7RR4CfYs_jlyLNYs04ah4NAQ3ZwJeK7A130_provenance.
- NP44019.RAgu1iVzD4DNdHPg05g6hp0dmWkbOoAZgHxzBpO5jy5s8130_assertion description "[Genotyping of the G1138A mutation of the FGFR3 gene in patients with achondroplasia using high-resolution melting analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44019.RAgu1iVzD4DNdHPg05g6hp0dmWkbOoAZgHxzBpO5jy5s8130_provenance.
- NP44020.RAu_Y9XZ47YD5o4JxTXVMUtXRjQvV5fI6b670WeTkFNRQ130_assertion description "[FGFR3 P250R mutation increases the risk of reoperation in apparent 'nonsyndromic' coronal craniosynostosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44020.RAu_Y9XZ47YD5o4JxTXVMUtXRjQvV5fI6b670WeTkFNRQ130_provenance.
- NP44024.RAmJo0RY-70g0yHPerN9Hb8S8-kfFC17vcvwxx4StRjtA130_assertion description "[We performed mutational analysis on 164 infants with isolated, single-suture craniosynostosis for mutations in TWIST1, the IgIIIa exon of FGFR1, the IgIIIa and IgIIIc exons of FGFR2, and the Pro250Arg site of FGFR3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44024.RAmJo0RY-70g0yHPerN9Hb8S8-kfFC17vcvwxx4StRjtA130_provenance.
- NP44036.RAoik3h8_eNu3Ba10GlVExPQ5AVfFCAtalfVKG9byu0I4130_assertion description "[Association studies of genetic polymorphism, environmental factors and their interaction in ischemic stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44036.RAoik3h8_eNu3Ba10GlVExPQ5AVfFCAtalfVKG9byu0I4130_provenance.
- NP44045.RAl_OVh6kw6L9VI7w0NEuDRnqp4k1dY-fRPFvarzPShXU130_assertion description "[Genetic polymorphisms of clotting factors and coronary heart disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44045.RAl_OVh6kw6L9VI7w0NEuDRnqp4k1dY-fRPFvarzPShXU130_provenance.
- NP44047.RAnBIhv1Pvl46ax1p8vrHbpYtdpiqIu6_HydbPgn50mzs130_assertion description "[ Chinese patients with UA had increased frequencies of GP Ib alpha C/B genotype and Bbeta fibrinogen 448A allele. These data suggest that some genetic factors may influence the development of UA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44047.RAnBIhv1Pvl46ax1p8vrHbpYtdpiqIu6_HydbPgn50mzs130_provenance.
- NP44048.RAvaDotNfdPsMIZ5T5tpC5lvRtre-8yvzBcp9Bi4oxDUA130_assertion description "[We identified common SNPs and haplotypes on FGA/FGB genes, explaining the interindividual and intraindividual variability of fibrinogen levels, in patients with a history of myocardial infarction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44048.RAvaDotNfdPsMIZ5T5tpC5lvRtre-8yvzBcp9Bi4oxDUA130_provenance.
- NP44050.RAg9ph5X-gT5y30iS3rWT_wS58ITW8rpn6lapOHmXX0xI130_assertion description "[among all the investigated polymorphisms only the 5709G and eNOS4a alleles seem to confer protection against MI in the young age of Sardinian people.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44050.RAg9ph5X-gT5y30iS3rWT_wS58ITW8rpn6lapOHmXX0xI130_provenance.
- NP44052.RAgNIZSCweOAlK88mzuhL52By2dUYnVO-Mv3LkJtBR1Vk130_assertion description "[Modification of the interleukin-6 response to air pollution by interleukin-6 and fibrinogen polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44052.RAgNIZSCweOAlK88mzuhL52By2dUYnVO-Mv3LkJtBR1Vk130_provenance.
- NP44054.RAgnYuBuqgDdChBkRgrjQAeChgkjn41zDlf_1WYc8-6QQ130_assertion description "[In conclusion, fibrinogen haplotypes, but not SNPs in isolation, are associated with variation in risk of MI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44054.RAgnYuBuqgDdChBkRgrjQAeChgkjn41zDlf_1WYc8-6QQ130_provenance.
- NP44068.RAgKiM-GLugbe3bKB1x6wDaZPtjrjGNhm0Cgm3haAnCP0130_assertion description "[ The above findings indicated that genetic variations in PAI-1 and beta fibrinogen loci might represent risk factors for glomerular microthrombosis in LN. They may have synergetic impact and present gene dosage effect on the susceptibility to this pathological subphenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44068.RAgKiM-GLugbe3bKB1x6wDaZPtjrjGNhm0Cgm3haAnCP0130_provenance.
- NP44069.RAj-L8mSLbZchrToq5s3VsIZFVXouSgfX43pVfWeF-7zs130_assertion description "[ The above findings indicated that genetic variations in PAI-1 and beta fibrinogen loci might represent risk factors for glomerular microthrombosis in LN. They may have synergetic impact and present gene dosage effect on the susceptibility to this pathological subphenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44069.RAj-L8mSLbZchrToq5s3VsIZFVXouSgfX43pVfWeF-7zs130_provenance.
- NP44071.RAopHGM5krV22buZTRnVx-ZN7L3wiUlBYmR-Qny0VFuXk130_assertion description "[ The above findings indicated that genetic variations in PAI-1 and beta fibrinogen loci might represent risk factors for glomerular microthrombosis in LN. They may have synergetic impact and present gene dosage effect on the susceptibility to this pathological subphenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44071.RAopHGM5krV22buZTRnVx-ZN7L3wiUlBYmR-Qny0VFuXk130_provenance.
- NP44073.RAvoS68lmUYAeBRfUBYqEq6t-J2yo5YP821PLrTsn2_fE130_assertion description "[The combination of prothrombotic polymorphisms may help to predict MI in patients with advanced CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44073.RAvoS68lmUYAeBRfUBYqEq6t-J2yo5YP821PLrTsn2_fE130_provenance.
- NP44076.RAvTsbLdeWzNu451zuhRwvPjff2K1zDLMc3UiRxbo7-Lg130_assertion description "[The results of our study suggest that, in addition to prothrombotic mutations such as Factor V Leiden, single-nucleotide polymorphisms should be considered in all children with congenital cardiac malformations who develop thrombosis. Malformations of the]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44076.RAvTsbLdeWzNu451zuhRwvPjff2K1zDLMc3UiRxbo7-Lg130_provenance.
- NP44080.RAjaJ6Ei6c4Dag1qVcYzqp2ciubu4py3-0eOygXb5J2RA130_assertion description "[The data suggest that susceptibility to ambient particulate matter may be partly genetically determined by polymorphisms that alter early physiological responses such as transcription of fibrinogen.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44080.RAjaJ6Ei6c4Dag1qVcYzqp2ciubu4py3-0eOygXb5J2RA130_provenance.
- NP44082.RAh3rk7iWW8R4rjqa3R5qHMn8YHL8C_Ia9Y9e-mboiazA130_assertion description "[A haplotype analysis did not reveal a link between genetic variations in the fibrinogen gene region and myocardial infarction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44082.RAh3rk7iWW8R4rjqa3R5qHMn8YHL8C_Ia9Y9e-mboiazA130_provenance.
- NP44088.RAnQ4nug3ksoos2_8luCQ1OftZ-xgT1h6jFM_GgLsk2ZM130_assertion description "[ A modest association between FEZ1 and schizophrenia suggests that this gene and the DISC1-mediated molecular pathway might play roles in the development of schizophrenia, with FEZ1 affecting only a small subset of Japanese schizophrenia patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44088.RAnQ4nug3ksoos2_8luCQ1OftZ-xgT1h6jFM_GgLsk2ZM130_provenance.
- NP44089.RAo6YSYnEBZMOD6OLgu7swFvLFaK0rHfxcm9a_UMRcq3M130_assertion description "[Identification of neuroglycan C and interacting partners as potential susceptibility genes for schizophrenia in a Southern Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44089.RAo6YSYnEBZMOD6OLgu7swFvLFaK0rHfxcm9a_UMRcq3M130_provenance.
- NP44091.RAoeC6BUgj8Bn2NT8aKrIiqxwO0ZRehrB7v_VGQIunXQI130_assertion description "[Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: the SzGene database.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44091.RAoeC6BUgj8Bn2NT8aKrIiqxwO0ZRehrB7v_VGQIunXQI130_provenance.
- NP44092.RAuZo4FlShyYCHXJreUUv1FN3lIpS2VGBS3q_uyA6uI8A130_assertion description "[Genetic association and post-mortem brain mRNA analysis of DISC1 and related genes in schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44092.RAuZo4FlShyYCHXJreUUv1FN3lIpS2VGBS3q_uyA6uI8A130_provenance.
- NP44102.RAtSlvGTKcMpTrKYfMccc9eMX7sn-BHLQbeiRelvjdw7o130_assertion description "[ The results of this explorative study support the view that the FcgammaRIIa/IIIa and IIIb polymorphisms constitute factors influencing clinical manifestations and the disease course of SLE but do not represent genetic risk factors for the occurrence of SLE. Higher frequencies of clinical symptoms, haematological and immunological abnormalities as well as an earlier onset of clinical symptoms, haematological and immunological markers of active disease were found in patients with the IIA-R/R131 genotype and the double negative and triple negative genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44102.RAtSlvGTKcMpTrKYfMccc9eMX7sn-BHLQbeiRelvjdw7o130_provenance.
- NP44104.RAm5fnRZ1cytKsXcPQ37ZvljMJfUSkFeLloTxAERm4ngE130_assertion description "[ The FcgammaRIIa-R/H131 polymorphism represents a significant risk factor for SLE but has no clear effect on susceptibility for lupus nephritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44104.RAm5fnRZ1cytKsXcPQ37ZvljMJfUSkFeLloTxAERm4ngE130_provenance.
- NP44108.RAqI13kKoU0MWMQwL-YEtz_RJLfKudGdUulhvr4t4ykQ8130_assertion description "[Common genetic variants in the interleukin-6 and chitotriosidase genes are associated with the risk for serious infection in children undergoing therapy for acute myeloid leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44108.RAqI13kKoU0MWMQwL-YEtz_RJLfKudGdUulhvr4t4ykQ8130_provenance.
- NP44115.RAuZBS-d7xi_XhbeBBVv7nqr0M8AFq9Of519Ps5E2cJFI130_assertion description "[Influence of variants of Fc gamma receptors IIA and IIIA on the American College of Rheumatology and European League Against Rheumatism responses to anti-tumour necrosis factor alpha therapy in rheumatoid arthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44115.RAuZBS-d7xi_XhbeBBVv7nqr0M8AFq9Of519Ps5E2cJFI130_provenance.
- NP44120.RAhtZpyWUQzsL5BpTiB8Z0JZBbvVCJHhnVOSLpnoimiic130_assertion description "[ These results suggest that the Fc gamma RIIIB NA1/NA1 may be a risk indicator for the susceptibility of the EOP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44120.RAhtZpyWUQzsL5BpTiB8Z0JZBbvVCJHhnVOSLpnoimiic130_provenance.
- NP44122.RAi7letKuf8OV2qeMMdt2ajPJZqqH487jlXbtxwdoJpcg130_assertion description "[ The Fc gamma RIIA-R/R131 genotype may be one of the contributors for the increased susceptibility to severe CP in Chinese Han nationality.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44122.RAi7letKuf8OV2qeMMdt2ajPJZqqH487jlXbtxwdoJpcg130_provenance.
- NP44137.RAqU500l937M3hkS5Mpg8AMxkoG1NsHQYd8jKudzzUwp0130_assertion description "[ The FcgammaRIIA-R/H-131 polymorphism may be an important marker in determining predisposition to RF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44137.RAqU500l937M3hkS5Mpg8AMxkoG1NsHQYd8jKudzzUwp0130_provenance.
- NP44144.RAnHTZ3p79D2p40PQC3DGpV4NtEZ5DWjgQ48fUGZiGmYk130_assertion description "[Genome-wide association study identifies FCGR2A as a susceptibility locus for Kawasaki disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44144.RAnHTZ3p79D2p40PQC3DGpV4NtEZ5DWjgQ48fUGZiGmYk130_provenance.
- NP44146.RAr-vIn4VMKkxE4XRXM84iid3owk85OQRMUFgj1hGNPzQ130_assertion description "[Results suggest that FcgammaRIII genotypes may represent mild disease-modifying factors in GBS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44146.RAr-vIn4VMKkxE4XRXM84iid3owk85OQRMUFgj1hGNPzQ130_provenance.
- NP44149.RAswJZXQigj_67yVRbdM3HhUtuf6pbdUkFSGYm4b9N_3w130_assertion description "[These observations underscore the importance of Fcgamma receptor-mediated cell clearance in childhood ITP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44149.RAswJZXQigj_67yVRbdM3HhUtuf6pbdUkFSGYm4b9N_3w130_provenance.
- NP44153.RAiSBf48DOLTMNcBqBRsWar6UD5-fJRaQr9NAdd6WHcPI130_assertion description "[This is the first evidence for an association between CD32 polymorphism and severe malaria and provides an example of balancing selective pressures from different infectious diseases operating at the same genetic locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44153.RAiSBf48DOLTMNcBqBRsWar6UD5-fJRaQr9NAdd6WHcPI130_provenance.
- NP44160.RAkGfuzuoqUtSL5yXrNAFMbp0uEqTT_Jt5DftVx0wqEvo130_assertion description "[Human Fc gamma receptor IIA (FcgammaRIIA) genotyping and association with systemic lupus erythematosus (SLE) in Chinese and Malays in Malaysia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44160.RAkGfuzuoqUtSL5yXrNAFMbp0uEqTT_Jt5DftVx0wqEvo130_provenance.
- NP44164.RAsiRsb4Y1zwnSnDTbqbqL-evuCnq5UgKiwjz6L0Hd0u4130_assertion description "[Polymorphisms in candidate asthma genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44164.RAsiRsb4Y1zwnSnDTbqbqL-evuCnq5UgKiwjz6L0Hd0u4130_provenance.
- NP44166.RAkZ7aRvMODTl1b1zsPZ_5fKCJfe-cFHbIBjGjEbPgYgQ130_assertion description "[ There were interethnic differences in the frequencies of the G variant among Chinese, Malay, and Indian populations. The E237G polymorphism of FcsRI beta may be a risk factor for asthma in the Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44166.RAkZ7aRvMODTl1b1zsPZ_5fKCJfe-cFHbIBjGjEbPgYgQ130_provenance.
- NP44177.RAmwxEiUd81ImMyUadmFw-ZCn0pqxQ3sYLpP330E7xeGg130_assertion description "[Identification of fibrillin-1 gene mutations in Marfan syndrome by high-resolution melting analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44177.RAmwxEiUd81ImMyUadmFw-ZCn0pqxQ3sYLpP330E7xeGg130_provenance.
- NP44183.RAvHeWlyZI4MRCxcVuWcqb90spmUJB6dZvnjgFXtKqd50130_assertion description "[Association of 5'-untranslated region of the Fibrillin-1 gene with Japanese scleroderma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44183.RAvHeWlyZI4MRCxcVuWcqb90spmUJB6dZvnjgFXtKqd50130_provenance.
- NP44186.RAjGpZbhXVqTdPQhI1t7F7NcYT08UPfag8jAWX5kpRcW4130_assertion description "[In contrast with data from Choctaw and Japanese patients, no association was detected between the polymorphic markers of FBN1 and SSc in 2 European Caucasian populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44186.RAjGpZbhXVqTdPQhI1t7F7NcYT08UPfag8jAWX5kpRcW4130_provenance.
- NP44187.RAizPVw2UpuKQG2o-UCRsfz-hWRHSLIpkkZwb-zuF1xGI130_assertion description "[Patients with MVP have higher frequencies of FBN1 exon 15 TT and exon 27 GG genotypes, which supports a role of the FBN1 exon 15 and 27 polymorphisms in determining the risk of MVP among the Chinese population in Taiwan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44187.RAizPVw2UpuKQG2o-UCRsfz-hWRHSLIpkkZwb-zuF1xGI130_provenance.
- NP44189.RAmQRIbNLKkommVbgCoIAPN_RkMDsDzOr2vNn0TJMg1IM130_assertion description "[Association of 5'-untranslated region of the Fibrillin-1 gene with Japanese scleroderma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44189.RAmQRIbNLKkommVbgCoIAPN_RkMDsDzOr2vNn0TJMg1IM130_provenance.
- NP44190.RAmkH5Oc960JVaCjXgDIckBI_e032F8vmT-HkHUH5AS9s130_assertion description "[ A 2-cM haplotype on chromosome 15q that contains FBN1 is associated with scleroderma in Choctaw Native Americans from Oklahoma. This haplotype may have been inherited from common founders about 10 generations ago and may contribute to the high prevalence of SSc that is now seen.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44190.RAmkH5Oc960JVaCjXgDIckBI_e032F8vmT-HkHUH5AS9s130_provenance.
- NP44194.RAmEvtfXtMKfCGEQ_NpTtwGVi1pk2EzWr0HlgvyT38nZA130_assertion description "[The results suggest that chromosomes with B allele have a genetic background that reduces susceptibility to MS, particularly in the familial forms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44194.RAmEvtfXtMKfCGEQ_NpTtwGVi1pk2EzWr0HlgvyT38nZA130_provenance.
- NP44197.RAsnIMdEwKM_lH23N5Iq9wVY5VLptDaO8tbKyuf2_ey6k130_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." NP44197.RAsnIMdEwKM_lH23N5Iq9wVY5VLptDaO8tbKyuf2_ey6k130_provenance.
- NP44201.RAt1Lw8BsPC-fXh-DnV_IXknp_ErJjqsJq1rLrN3Dvzmk130_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." NP44201.RAt1Lw8BsPC-fXh-DnV_IXknp_ErJjqsJq1rLrN3Dvzmk130_provenance.
- NP44205.RAs1pCwYZJBJOYpfD97pmAgTxrKYj0kNtju69qA3fLr7g130_assertion description "[ Genetic polymorphisms in the death pathway genes FAS and FASL appear to be associated with an increased risk of developing esophageal squamous-cell carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44205.RAs1pCwYZJBJOYpfD97pmAgTxrKYj0kNtju69qA3fLr7g130_provenance.
- NP44217.RAmeYpQ52UqjCFvJz2MpsGoIaMv03Ru2ccSOzsSSCyWJA130_assertion description "[This is the first study on the role of Fas and FasL polymorphisms in cervical cancer in African populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44217.RAmeYpQ52UqjCFvJz2MpsGoIaMv03Ru2ccSOzsSSCyWJA130_provenance.
- NP44218.RApNOjcsaebl9m_L8oqQtz7KVEpPa4P9DEWvJ8M_fj8DY130_assertion description "[ Using the same methods used in the present studies (PCR/SSCP), one group of investigators identified a structural defect of the FasL molecule in 1 of 75 SLE patients evaluated. Among the 143 SLE patients in the present study, however, we did not identify any mutations or polymorphisms of the FasL gene. Our results suggest that a FasL defect is not the major contributing factor in the pathogenesis of SLE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44218.RApNOjcsaebl9m_L8oqQtz7KVEpPa4P9DEWvJ8M_fj8DY130_provenance.
- NP44221.RAuPUEnNS5_ep7QbMr0yXVJl_lEy5ARWIAS0oCfFTLlDM130_assertion description "[We found no strong evidence of association for any of these loci with AD in this population. While the possibility exists that the genes analysed are involved in AD (ie they have weak effects and/or are population specific), results reinforce the need for extensive replication studies if we are to be successful in defining true risk factors in complex diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44221.RAuPUEnNS5_ep7QbMr0yXVJl_lEy5ARWIAS0oCfFTLlDM130_provenance.
- NP44223.RAnykuyGIRiwITUBCgVkZjtAxvR0a9AHHMW4GVXWexI9o130_assertion description "[These results imply that TNFRSF6, in interaction with APOE4, is a genetic risk factor for sporadic EOAD. Hence, the AD risk contributed by APOE4 could be mechanistically related to a pathway in common with FAS-mediated apoptosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44223.RAnykuyGIRiwITUBCgVkZjtAxvR0a9AHHMW4GVXWexI9o130_provenance.
- NP44224.RApOq9VTMwnmpYG3Ni9RkRLKhXG42Jgb7jXJ1jagMG4JQ130_assertion description "[Fas antigen and sporadic Alzheimer's disease in Southern Italy: evaluation of two polymorphisms in the TNFRSF6 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44224.RApOq9VTMwnmpYG3Ni9RkRLKhXG42Jgb7jXJ1jagMG4JQ130_provenance.
- NP44226.RAt-RKdw5lXXPJuGvh2jb5AC9jlYaasRI93E5RgjkCFnY130_assertion description "[Polymorphisms of fas gene: relationship with Alzheimer's disease and cognitive decline.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44226.RAt-RKdw5lXXPJuGvh2jb5AC9jlYaasRI93E5RgjkCFnY130_provenance.
- NP44230.RAomc9jbEI0oS5Lng1jS95ZQgEJl79_akYUn2yEXo2HDI130_assertion description "[ Overall, our findings suggest that Apo-1/Fas promoter gene polymorphisms are not conclusively related to susceptibility to MS or the clinical characteristics of Japanese patients with MS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44230.RAomc9jbEI0oS5Lng1jS95ZQgEJl79_akYUn2yEXo2HDI130_provenance.
- NP44235.RAgtw4yd8bilcNf9FjIXV443j0Gud-MAq1tl99tWERzvk130_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." NP44235.RAgtw4yd8bilcNf9FjIXV443j0Gud-MAq1tl99tWERzvk130_provenance.
- NP44237.RAhzJ4Q-m3q-puhyRcdoQykf6ZZkNTv05P_Kq8rcFJ_sc130_assertion description "[ The FAS -1377A/-670A haplotype in combination with FASL -844C is associated with cervical carcinogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44237.RAhzJ4Q-m3q-puhyRcdoQykf6ZZkNTv05P_Kq8rcFJ_sc130_provenance.
- NP44238.RApytC6YdhCRWOZOZvqy_G22DnBc9SPxfYf0iLsiVBg_0130_assertion description "[ Fas gene promoter -670 polymorphism (A/G) may be closely associated with cervical carcinogenesis in a Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44238.RApytC6YdhCRWOZOZvqy_G22DnBc9SPxfYf0iLsiVBg_0130_provenance.
- NP44239.RAlHYSoHOxdmpWcWAk0c3n1hiGasCN4QYiGM1I0BuWUWA130_assertion description "[New approach reveals CD28 and IFNG gene interaction in the susceptibility to cervical cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44239.RAlHYSoHOxdmpWcWAk0c3n1hiGasCN4QYiGM1I0BuWUWA130_provenance.
- NP44243.RAovXP4b5juf7bYNotnt30fhHEkchBu0c-Dt1imdoEyuM130_assertion description "[Genetic polymorphism in the FAS gene may account for some of the histopathological variability in chronic hepatitis C.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44243.RAovXP4b5juf7bYNotnt30fhHEkchBu0c-Dt1imdoEyuM130_provenance.
- NP44246.RAigThTRglNEYyUcIQ5v2Hagq5sCcZl0CFMPqcnDg3f4Q130_assertion description "[These studies identify single locus associations with preterm birth for both maternal and fetal genotypes in two populations of European ancestry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44246.RAigThTRglNEYyUcIQ5v2Hagq5sCcZl0CFMPqcnDg3f4Q130_provenance.
- NP44248.RAppRcVIT0anhScwwIkUqFGQTw-daRSQmrfr521yIfAAc130_assertion description "[ Genetic polymorphisms in the death pathway genes FAS and FASL appear to be associated with an increased risk of developing esophageal squamous-cell carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44248.RAppRcVIT0anhScwwIkUqFGQTw-daRSQmrfr521yIfAAc130_provenance.
- NP44252.RAs1Rg6r5Ri92yEHtryOIk7-g0_G-Vgh_x9E9ulGCyQpE130_assertion description "[Germline genetic variations in drug action pathways predict clinical outcomes in advanced lung cancer treated with platinum-based chemotherapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44252.RAs1Rg6r5Ri92yEHtryOIk7-g0_G-Vgh_x9E9ulGCyQpE130_provenance.
- NP44253.RAvaPnoAeSbBfFt59c4EaWYE5EPzvsoBzlewNiY2bRx7E130_assertion description "[Apoptosis gene polymorphisms, age, smoking and the risk of non-small cell lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44253.RAvaPnoAeSbBfFt59c4EaWYE5EPzvsoBzlewNiY2bRx7E130_provenance.
- NP44262.RAum_8_Xtom7wz9pmMJ5B34m9oVTojLUEVqe07isN4Ms0130_assertion description "[ Fas promoter -670A/G polymorphism was significantly associated with SLE, suggesting a possibility that Fas promoter contributes, at least in part, to the pathogenesis of SLE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44262.RAum_8_Xtom7wz9pmMJ5B34m9oVTojLUEVqe07isN4Ms0130_provenance.
- NP44264.RAp5-8nphzQPrzILeMdgZXMRCOFMxhkFKPe05Ina1fVQ4130_assertion description "[ Fas promoter -670A/G polymorphism was significantly associated with SLE, suggesting a possibility that Fas promoter contributes, at least in part, to the pathogenesis of SLE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44264.RAp5-8nphzQPrzILeMdgZXMRCOFMxhkFKPe05Ina1fVQ4130_provenance.
- NP44267.RAifhzb83-VPe8ZMZYOSpdE8W1wcLtX8ceTM62eM6kVhY130_assertion description "[Frequency of Fanconi anemia in Brazil and efficacy of screening for the FANCA 3788-3790del mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44267.RAifhzb83-VPe8ZMZYOSpdE8W1wcLtX8ceTM62eM6kVhY130_provenance.
- NP44268.RAhRFSQUF-QRJw0J22DKaJnm2YswrhDKpaOv1Lue7vvl8130_assertion description "[Taken together these data support the assertion that inherited mutations in FANCC can predispose to pancreatic cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44268.RAhRFSQUF-QRJw0J22DKaJnm2YswrhDKpaOv1Lue7vvl8130_provenance.
- NP44270.RAiKcS7FK85u7qWkezvVP1CkbhaAB9RaHPjFpBmpKZ4E8130_assertion description "[By logistic and multiple regression analysis, one insertion/deletion polymorphism in the 3' end (c.634+483delT) of FABP3 appeared to be weakly associated with increased risk of type 2 diabetes (OR=1.78-1.94, P=0.03-0.04) and waist/hip ratio (WHR) (P=0.03).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44270.RAiKcS7FK85u7qWkezvVP1CkbhaAB9RaHPjFpBmpKZ4E8130_provenance.
- NP44274.RAlyYsUYgC8KBYUkEgBeOVq6yg5rIgJAKqMFhODiu9UTI130_assertion description "[We investigated the association of the A54T polymorphism of the FABP2 gene with the metabolic syndrome defined according to the diagnostic criteria recommended by the IDF in 2005, in our region (Marosvsrhely - Tg.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44274.RAlyYsUYgC8KBYUkEgBeOVq6yg5rIgJAKqMFhODiu9UTI130_provenance.
- NP44275.RAt_Gb184ppYfG9HikUD5QmwyoTPouEK1yhV6hSDakCB8130_assertion description "[Our results suggest that FABP2, IPF1, FABP1, ROS1, ADIPOQ, ALOX5AP, NOS3, and LGALS2 are susceptibility loci for atherothrombotic cerebral infarction among Japanese individuals with metabolic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44275.RAt_Gb184ppYfG9HikUD5QmwyoTPouEK1yhV6hSDakCB8130_provenance.
- NP44276.RAqHY02MbLqfVznYlA2JDzRjGhpvN5x0UbI3Su3mugl-4130_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." NP44276.RAqHY02MbLqfVznYlA2JDzRjGhpvN5x0UbI3Su3mugl-4130_provenance.
- NP44279.RAsIGeMjfKr1-uyDdOo-sJiDkbu42fnPHvqd1RMnYqFs4130_assertion description "[The objective of the present study was to investigate the role of ADMA and the FABP2 A54T polymorphism in carotid atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44279.RAsIGeMjfKr1-uyDdOo-sJiDkbu42fnPHvqd1RMnYqFs4130_provenance.
- NP44280.RAliCig6CIwSxjEc2ZsBDcVCkboOQ7oCkmg0w_57d8G0M130_assertion description "[It was concluded that FABP2 genotype influences insulin sensitivity independent of body composition, habitual physical activity levels, and HRT status in postmenopausal white women]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44280.RAliCig6CIwSxjEc2ZsBDcVCkboOQ7oCkmg0w_57d8G0M130_provenance.
- NP44281.RApm_XD9GeLnvO08QGipjCyOr-xQlgHNtIy7IiRrIGmsE130_assertion description "[Genetic polymorphism of pyruvate dehydrogenase kinase 4 (PDK4), paraoxonase 2 (PON2), and fatty acid binding protein 2 (FABP2) in the NIDDM population of Senegal.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44281.RApm_XD9GeLnvO08QGipjCyOr-xQlgHNtIy7IiRrIGmsE130_provenance.
- NP44283.RAjRhe5xwaj5wjq_7zMEixrQ48_0p4W6FC0vvUAI9dce0130_assertion description "[Type 2 diabetes mellitus: association study of five candidate genes in an Indian population of Guadeloupe, genetic contribution of FABP2 polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44283.RAjRhe5xwaj5wjq_7zMEixrQ48_0p4W6FC0vvUAI9dce0130_provenance.
- NP44284.RAlgOezjw-kOxRkJxkvAzCrfBDwDlJTCrGroq9AjGNj-c130_assertion description "[Codon-54 polymorphism of the fatty acid-binding protein 2 gene is associated with elevation of fasting and postprandial triglyceride in type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44284.RAlgOezjw-kOxRkJxkvAzCrfBDwDlJTCrGroq9AjGNj-c130_provenance.
- NP44286.RAjgXZRUkL2rr462utIFLYsrFf8aUpFpiUwE1djSBnnas130_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." NP44286.RAjgXZRUkL2rr462utIFLYsrFf8aUpFpiUwE1djSBnnas130_provenance.
- NP44288.RAu8Pk3syFW6dMn6Bpqru9maEC4s-ZBfkejxTxELB222s130_assertion description "[ Our findings suggest an involvement of the FABP2 (A54T) gene polymorphism in the pathogenesis of CVD. The FABP2 T54 allele appears to be a genetic susceptibility marker for TIA and non-cardioembolic infarction at younger onset.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44288.RAu8Pk3syFW6dMn6Bpqru9maEC4s-ZBfkejxTxELB222s130_provenance.
- NP44294.RAkcQ-Hg9HR19-OkqvAeEAsQlrgED_xc6sLBiDllDUXkk130_assertion description "[ The A54T polymorphism at the FABP2 locus is a risk factor for insulin resistance in a Caucasian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44294.RAkcQ-Hg9HR19-OkqvAeEAsQlrgED_xc6sLBiDllDUXkk130_provenance.
- NP44296.RAsYcZe4W_XikZMkf1tZi95J6Nnjp_p059qKFmCr6thNc130_assertion description "[The T 54 allele of the intestinal fatty acid-binding protein 2 is associated with a parental history of stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44296.RAsYcZe4W_XikZMkf1tZi95J6Nnjp_p059qKFmCr6thNc130_provenance.
- NP44297.RAmzVx84ynSGGgv8PNaiZjRVy_yfT0V92_KYqJivh0xsc130_assertion description "[ These results suggest a role for the FAAH 385 A/A missense polymorphism as an endocannabinoid risk factor in overweight/obesity and may provide indirect evidence to support cannabinoid antagonist treatment strategies in overweight disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44297.RAmzVx84ynSGGgv8PNaiZjRVy_yfT0V92_KYqJivh0xsc130_provenance.
- NP44298.RAgsmJCgrrJra1q0sNM2Gh9qbTynl16Q-DSgKixXxDbss130_assertion description "[We initially assessed association of five single nucleotide polymorphisms (SNPs) in FAAH with early onset extreme obesity in up to 521 German obese children and both parents.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44298.RAgsmJCgrrJra1q0sNM2Gh9qbTynl16Q-DSgKixXxDbss130_provenance.
- NP44302.RAqT57qvUB597r6ZOHdsyvc8mMG0FVaazdfH8969y_3d4130_assertion description "[ Using the above polymorphic markers of factors VIII and IX genes, a diagnosis could be made in the majority of families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44302.RAqT57qvUB597r6ZOHdsyvc8mMG0FVaazdfH8969y_3d4130_provenance.
- NP44306.RAsm2IjPIUCqVlsvfBvmNVxJoWpzHjASz6lM9Vxm2ffts130_assertion description "[A comparison of the heterozygosity rates of these three markers with the other ethnic groups showed that Indian population had almost similar pattern with the Caucasians and American blacks but differed significantly from the Orientals including Japanese, Chinese and Malays.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44306.RAsm2IjPIUCqVlsvfBvmNVxJoWpzHjASz6lM9Vxm2ffts130_provenance.
- NP44308.RAjsPcnQoYrGlS8-w7tOfuytxbfnZoYfXjqjB4JdYM2QU130_assertion description "[In conclusion, high FVIII levels and non-O blood groups, likely those with the A(1) allele, are independent risk factors for venous thromboembolism and should be considered in evaluating of thrombophilia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44308.RAjsPcnQoYrGlS8-w7tOfuytxbfnZoYfXjqjB4JdYM2QU130_provenance.
- NP44311.RAsfqyxl9Bt5nf7RA_JqHnLYqruVPawa6x4UsPfPPah50130_assertion description "[All mutation types detected were in agreement with the severe hemophilia A phenotype, most likely leading to a deficiency of and predisposition to the development of alloantibodies against FVIII.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44311.RAsfqyxl9Bt5nf7RA_JqHnLYqruVPawa6x4UsPfPPah50130_provenance.
- NP44315.RAjuBipno5Kdn_sEX8FU5V0J0fQb3OV1O9CeXjsAxLJ9w130_assertion description "[Factor VIII genotype and inhibitor development in patients with haemophilia A: highest risk in patients with splice site mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44315.RAjuBipno5Kdn_sEX8FU5V0J0fQb3OV1O9CeXjsAxLJ9w130_provenance.
- NP44329.RAnvhfT74KAfpXDt47EdYj0Nr5D80fLHwi7zNm3PYI01Q130_assertion description "[Influence of polymorphisms in the factor VII gene promoter on activated factor VII levels and on the risk of myocardial infarction in advanced coronary atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44329.RAnvhfT74KAfpXDt47EdYj0Nr5D80fLHwi7zNm3PYI01Q130_provenance.
- NP44334.RAuaXz07hkC8bki7xDrglqnWqUBR3oNPJdJmL4gw7ekm4130_assertion description "[According to our results, the FVII -402A allele seems to increase the risk of early ischemic cerebrovascular events, whereas the 353R>Q, G-401T, and -323ins/del sequence variations, which are in close linkage disequilibrium, apparently do not influence the risk of stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44334.RAuaXz07hkC8bki7xDrglqnWqUBR3oNPJdJmL4gw7ekm4130_provenance.
- NP44335.RApFQ_umxE5pZOHM1T-d9OuY8zCEmHZHd7uAY39UQl4rI130_assertion description "[This study shows that for some genes, further studies are unnecessary, whereas for others, no more enrollments are needed. The impact of certain genotypes must be examined in relation to other established risk factors and potentially new therapeutic strategies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44335.RApFQ_umxE5pZOHM1T-d9OuY8zCEmHZHd7uAY39UQl4rI130_provenance.
- NP44336.RAsogth_7I-jDuYGxBuiyQlrOgqyroIpZMz75_BUadIi4130_assertion description "[Joint effect of G1691A factor V point mutation and factor VII Arg/Gln(353) gene polymorphism on the risk of premature coronary artery disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44336.RAsogth_7I-jDuYGxBuiyQlrOgqyroIpZMz75_BUadIi4130_provenance.
- NP44341.RAhkE4HMMQDRckzOA5ohwn_vaol5hLVSUx1NLlkrGt2Us130_assertion description "[Distributions of polymorphisms of genes of some components of hemostasis in patients with ischemic heart disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44341.RAhkE4HMMQDRckzOA5ohwn_vaol5hLVSUx1NLlkrGt2Us130_provenance.
- NP44343.RArGnFtuK-5Arkl0uVnjrnr_lUhYLYU_VwZjsZK_3g7Ts130_assertion description "[ The Q allele may be protective against premature MI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44343.RArGnFtuK-5Arkl0uVnjrnr_lUhYLYU_VwZjsZK_3g7Ts130_provenance.
- NP44347.RAgLCI9LuxXo2JYOU16uiNMANeLcLTMD-MTab_bSfpQBo130_assertion description "[among all the investigated polymorphisms only the 5709G and eNOS4a alleles seem to confer protection against MI in the young age of Sardinian people.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44347.RAgLCI9LuxXo2JYOU16uiNMANeLcLTMD-MTab_bSfpQBo130_provenance.