. . . . . . . "[In Caucasians, first-stage analysis of 254 haplotype-tagging SNPs in 15 LT pathway genes with follow-up of 19 variants in stage 2 revealed an LTA4H SNP (rs2540477) that increased risk of CAD (OR�=�1.2, 95% CI 1.1-1.5; p�=�0.003) and a PLA2G4A SNP (rs12746200) that decreased risk of CAD (OR�=�0.7, 95% CI 0.6-0.9; p�=�0.0007).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2017-02-19"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2017-10-17T13:15:27+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .