Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1246667.RAos1a8VFvPKJh4Plx5TKjHEsCjtB6lvsGbzi2HPNvSng130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1246667.RAos1a8VFvPKJh4Plx5TKjHEsCjtB6lvsGbzi2HPNvSng130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1246667.RAos1a8VFvPKJh4Plx5TKjHEsCjtB6lvsGbzi2HPNvSng130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1246667.RAos1a8VFvPKJh4Plx5TKjHEsCjtB6lvsGbzi2HPNvSng130_provenance.
- NP1246667.RAos1a8VFvPKJh4Plx5TKjHEsCjtB6lvsGbzi2HPNvSng130_assertion description "[Mutations in the valosin-containing protein (VCP) gene were first found to cause inclusion- body myopathy with early-onset Paget disease and frontotemporal dementia (IBMPFD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1246667.RAos1a8VFvPKJh4Plx5TKjHEsCjtB6lvsGbzi2HPNvSng130_provenance.
- NP1246667.RAos1a8VFvPKJh4Plx5TKjHEsCjtB6lvsGbzi2HPNvSng130_assertion evidence source_evidence_literature NP1246667.RAos1a8VFvPKJh4Plx5TKjHEsCjtB6lvsGbzi2HPNvSng130_provenance.
- NP1246667.RAos1a8VFvPKJh4Plx5TKjHEsCjtB6lvsGbzi2HPNvSng130_assertion SIO_000772 25492614 NP1246667.RAos1a8VFvPKJh4Plx5TKjHEsCjtB6lvsGbzi2HPNvSng130_provenance.
- NP1246667.RAos1a8VFvPKJh4Plx5TKjHEsCjtB6lvsGbzi2HPNvSng130_assertion wasDerivedFrom befree-2016 NP1246667.RAos1a8VFvPKJh4Plx5TKjHEsCjtB6lvsGbzi2HPNvSng130_provenance.
- NP1246667.RAos1a8VFvPKJh4Plx5TKjHEsCjtB6lvsGbzi2HPNvSng130_assertion wasGeneratedBy ECO_0000203 NP1246667.RAos1a8VFvPKJh4Plx5TKjHEsCjtB6lvsGbzi2HPNvSng130_provenance.
- befree-2016 importedOn "2016-02-19" NP1246667.RAos1a8VFvPKJh4Plx5TKjHEsCjtB6lvsGbzi2HPNvSng130_provenance.