. . . . . . . "[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 . . . . . "2017-02-19"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2017-10-17T13:17:08+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .