Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP654441.RAOw9P5E2cs-fmNoxtcQ8YnuG9cmuAM2GQfi2AlPG-CdQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP654441.RAOw9P5E2cs-fmNoxtcQ8YnuG9cmuAM2GQfi2AlPG-CdQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP654441.RAOw9P5E2cs-fmNoxtcQ8YnuG9cmuAM2GQfi2AlPG-CdQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP654441.RAOw9P5E2cs-fmNoxtcQ8YnuG9cmuAM2GQfi2AlPG-CdQ130_provenance.
- NP654441.RAOw9P5E2cs-fmNoxtcQ8YnuG9cmuAM2GQfi2AlPG-CdQ130_assertion description "[Inclusion body myopathy with Paget disease of the bone (PDB) and/or frontotemporal dementia (IBMPFD, OMIM 167320), is a progressive autosomal dominant disorder caused by mutations in the Valousin-containing protein (VCP, p97 or CDC48) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP654441.RAOw9P5E2cs-fmNoxtcQ8YnuG9cmuAM2GQfi2AlPG-CdQ130_provenance.
- NP654441.RAOw9P5E2cs-fmNoxtcQ8YnuG9cmuAM2GQfi2AlPG-CdQ130_assertion evidence source_evidence_literature NP654441.RAOw9P5E2cs-fmNoxtcQ8YnuG9cmuAM2GQfi2AlPG-CdQ130_provenance.
- NP654441.RAOw9P5E2cs-fmNoxtcQ8YnuG9cmuAM2GQfi2AlPG-CdQ130_assertion SIO_000772 18260132 NP654441.RAOw9P5E2cs-fmNoxtcQ8YnuG9cmuAM2GQfi2AlPG-CdQ130_provenance.
- NP654441.RAOw9P5E2cs-fmNoxtcQ8YnuG9cmuAM2GQfi2AlPG-CdQ130_assertion wasDerivedFrom befree-2016 NP654441.RAOw9P5E2cs-fmNoxtcQ8YnuG9cmuAM2GQfi2AlPG-CdQ130_provenance.
- NP654441.RAOw9P5E2cs-fmNoxtcQ8YnuG9cmuAM2GQfi2AlPG-CdQ130_assertion wasGeneratedBy ECO_0000203 NP654441.RAOw9P5E2cs-fmNoxtcQ8YnuG9cmuAM2GQfi2AlPG-CdQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP654441.RAOw9P5E2cs-fmNoxtcQ8YnuG9cmuAM2GQfi2AlPG-CdQ130_provenance.