. . . . . . . "[Furthermore, individuals carrying one or two MC1R nonsynonymous changes and GSTP1 rs1695 rare allele had an increased risk of developing MM (OR: 3�34, 95% CI: 1�42-8�09 and OR: 20�42, 95% CI: 2�80-417�42, respectively).]. 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 . "2017-10-17T13:14:27+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .