. . . . . . . "[heterozygous carriers of FVL who experience an episode of venous thromboembolism (VTE) have on average a 40% increased risk of recurrent VTE over non-carriers; risk is lower with heterozygosity of prothrombin G20210A mutation [review]]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2009-03-31"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2017-10-17T13:12:35+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .