. . . . . . . "[The majority of mutations responsible for autosomatic dominant optic atrophy are localized in OPA1 gene/locus is linked to 18q12.2-q12.3 (OPA4) and a third locus on 22q12.1-q13.1 (OPA5).]. 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 . "2017-10-17T13:19:25+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .