. . . . . . . "[The pathogenesis of DF is not completely understood even if a high prevalence (?85%) of CTNNB1 mutations discovered in sporadic DF underlies the importance of the Wnt/?-catenin pathway.]. 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 . "2017-10-17T13:11:49+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .