. . . . . . . . . . . . "[it is very likely that this novel mutation causes a complete loss of NKX2-5 function and haploinsufficiency is the pathophysiological mechanism underlying the autosomal-dominant inherited congenital heart disease in the family.]. 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 . "2014-10-02T12:33:03+02:00"^^ . . . . . . . . . . . "v2.1.0.0" . "v2.1.0" .