. . . . . . . "[A consistent fraction of cases carries de-novo SMARCB1/INI1 constitutional mutations in the setting of the 'rhabdoid tumor predisposition syndrome' and the outcome is worst in infant syndromic ATRT patients.]. 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 . "2017-10-17T13:16:19+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .