. . . . . . . "[However, we identified several regions with rare CNVs that were only observed in AN cases, including a recurrent 13q12 deletion (1.5?Mb) disrupting SCAS in two cases, and CNVs disrupting the CNTN6/CNTN4 region in several AN cases.]. 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 . "2017-10-17T13:19:08+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .