. . . . . . . . . . . . "[We propose that familial cortical myoclonus is a novel movement disorder that may be caused by mutation in NOL3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2015-02-27"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2015-08-25T14:45:52+02:00"^^ . . . . . . . . . . . "v3.0.0.0" . "v3.0.0" .