. . . . . . . . . . . . "[The involvement of congenital anomalies in all 16 clinically described patients with EP300 mutations (25% of which have been identified by hypothesis free methods, including microarray, exome, and whole-genome sequencing) is reviewed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2016-02-19"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2016-05-13T12:51:20+02:00"^^ . . . . . . . . . . . "v4.0.0.0" . "v4.0.0" .