. . . . . . . "[Based on the finding that a point mutation in the gene encoding ?-synuclein (?Syn) protein causes a rare familial form of PD, PARK1, it is now confirmed that ?Syn is a major component of Lewy bodies in patients with sporadic PD.]. 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 . "2017-10-17T13:16:20+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .