. . . . . . . . . . . . "[PINK1 mutations are rare in Norwegian patients with EOP and familial Parkinson's disease; however, the data suggest that some heterozygous mutations might increase the risk of developing Parkinson's disease ]. 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 . "2014-10-02T12:33:08+02:00"^^ . . . . . . . . . . . "v2.1.0.0" . "v2.1.0" .