. . . . . . . "[Founder deletion (p16-Leiden) in Dutch melanoma families does not account for the atypical nevus phenotype that segregates in both p16-Leiden carriers and non-carriers and is a risk factor and a precursor lesion for melanoma.]. 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 . "2017-10-17T13:11:27+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .