Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP939768.RABdXolKWIUWMpQGi2H6sq3xPxCz6fncGh4R6MTnr4N1Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP939768.RABdXolKWIUWMpQGi2H6sq3xPxCz6fncGh4R6MTnr4N1Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP939768.RABdXolKWIUWMpQGi2H6sq3xPxCz6fncGh4R6MTnr4N1Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP939768.RABdXolKWIUWMpQGi2H6sq3xPxCz6fncGh4R6MTnr4N1Q130_provenance.
- NP939768.RABdXolKWIUWMpQGi2H6sq3xPxCz6fncGh4R6MTnr4N1Q130_assertion description "[Mutations in the gene for valosin containing protein (VCP) cause autosomal dominant inclusion body myopathy associated with Paget disease and frontotemporal dementia (IBMPFD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP939768.RABdXolKWIUWMpQGi2H6sq3xPxCz6fncGh4R6MTnr4N1Q130_provenance.
- NP939768.RABdXolKWIUWMpQGi2H6sq3xPxCz6fncGh4R6MTnr4N1Q130_assertion evidence source_evidence_literature NP939768.RABdXolKWIUWMpQGi2H6sq3xPxCz6fncGh4R6MTnr4N1Q130_provenance.
- NP939768.RABdXolKWIUWMpQGi2H6sq3xPxCz6fncGh4R6MTnr4N1Q130_assertion SIO_000772 17618707 NP939768.RABdXolKWIUWMpQGi2H6sq3xPxCz6fncGh4R6MTnr4N1Q130_provenance.
- NP939768.RABdXolKWIUWMpQGi2H6sq3xPxCz6fncGh4R6MTnr4N1Q130_assertion wasDerivedFrom befree-20140225 NP939768.RABdXolKWIUWMpQGi2H6sq3xPxCz6fncGh4R6MTnr4N1Q130_provenance.
- NP939768.RABdXolKWIUWMpQGi2H6sq3xPxCz6fncGh4R6MTnr4N1Q130_assertion wasGeneratedBy ECO_0000203 NP939768.RABdXolKWIUWMpQGi2H6sq3xPxCz6fncGh4R6MTnr4N1Q130_provenance.
- befree-20140225 importedOn "2014-02-25" NP939768.RABdXolKWIUWMpQGi2H6sq3xPxCz6fncGh4R6MTnr4N1Q130_provenance.