. . . . . . . "[A patient with Inclusion body myopathy with Paget disease of bone and frontotemporal dementia carried a novel heterozygous base pair change, 47832C > T, in the VCP gene that resulted in substitution of an arginine residue by cysteine at position 93 (R93C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2009-03-31"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2017-10-17T13:17:11+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .