. . . . . . . "[The DFNB1 was clearly excluded as a molecular etiology in four (40%) subjects: other recessive deafness genes (N?=?3) accounted for SNHL and the causative gene for the other non-DFNB1 subject (N?=?1) was not identified.]. 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 . "2017-10-17T13:13:00+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .