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[Higher AP level corresponding to 3-rd degree AH in the group of patients with burdened familial anamnesis was associated with carriage of Asn allele of polymorphic marker Lysl98Asn of EDN1 gene (OR 2.24 95% CI 1.20-4.18, p=0.008), 4a allele of polymorphic marker 4a/4b of NOS3 gene (OR 2.23 C/1.29-3.83, p=0.002), genotype ArgArg of polymorphic marker Glnl92Arg of PON1 gene (OR 6.14 C71.46-25.67, p=0.01), T allele of polymorphic marker of C825T gene GNB3 (OR 1.75 C/1.11-2.76, p=0.01) and genotype AA of polymorphic marker A(A153)G of AT2R1 gene (OR 2.61 C/11.29-5.34, p=0.005).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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Gene-disease associations inferred from text-mining the literature.
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DisGeNET evidence - LITERATURE
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