. . . . . . . . . . . . "[With respect to human genetic diseases, GC-E mapped to mouse chromosome 11 within a syntenic region on human chromosome 17q13 that has been linked with loci for autosomal dominant retinitis pigmentosa and Leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2014-02-25"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2014-10-02T12:36:47+02:00"^^ . . . . . . . . . . . "v2.1.0.0" . "v2.1.0" .