. . . . . . . "[In recent studies, several mutations in the cytoplasmic sterile-?-motif (SAM) domain of human EPHA2 on chromosome 1p36 have been associated with hereditary cataracts in several families.]. 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 . "2017-10-17T13:12:16+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .