. . . . . . . "[NKX2.5 mutations occur in a small percentage of patients with various congenital heart diseases/. 5 mutations in non-homeodomain regions may be important in the development of human structural cardiac defects.]. 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 . "2017-10-17T13:11:48+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .