. . . . . . . . . . . . "[OCA3 (MIM 203290), a rare form of OCA and also known as `rufous/red albinism,` is associated with mutations in TYRP1 (encoding tyrosinase-related protein 1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2014-02-25"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2014-10-02T12:36:05+02:00"^^ . . . . . . . . . . . "v2.1.0.0" . "v2.1.0" .