. . . . . . . "[RBM10 encodes an RNA binding protein.Mutations in RBM10 are known to cause multiple congenital anomaly syndrome in male humans, the TARP syndrome.]. 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 . "2017-10-17T13:15:43+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .