Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP938256.RAbPeDKZ_un8l0N-6OK_ghCtVPMk1ep62wIUVjtPhv--U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP938256.RAbPeDKZ_un8l0N-6OK_ghCtVPMk1ep62wIUVjtPhv--U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP938256.RAbPeDKZ_un8l0N-6OK_ghCtVPMk1ep62wIUVjtPhv--U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP938256.RAbPeDKZ_un8l0N-6OK_ghCtVPMk1ep62wIUVjtPhv--U130_provenance.
- NP938256.RAbPeDKZ_un8l0N-6OK_ghCtVPMk1ep62wIUVjtPhv--U130_assertion description "[VCP mutations are known to cause inclusion body myopathy (IBM) with Paget's disease (PDB) and frontotemporal dementia (FTD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP938256.RAbPeDKZ_un8l0N-6OK_ghCtVPMk1ep62wIUVjtPhv--U130_provenance.
- NP938256.RAbPeDKZ_un8l0N-6OK_ghCtVPMk1ep62wIUVjtPhv--U130_assertion evidence source_evidence_literature NP938256.RAbPeDKZ_un8l0N-6OK_ghCtVPMk1ep62wIUVjtPhv--U130_provenance.
- NP938256.RAbPeDKZ_un8l0N-6OK_ghCtVPMk1ep62wIUVjtPhv--U130_assertion SIO_000772 22078486 NP938256.RAbPeDKZ_un8l0N-6OK_ghCtVPMk1ep62wIUVjtPhv--U130_provenance.
- NP938256.RAbPeDKZ_un8l0N-6OK_ghCtVPMk1ep62wIUVjtPhv--U130_assertion wasDerivedFrom befree-2016 NP938256.RAbPeDKZ_un8l0N-6OK_ghCtVPMk1ep62wIUVjtPhv--U130_provenance.
- NP938256.RAbPeDKZ_un8l0N-6OK_ghCtVPMk1ep62wIUVjtPhv--U130_assertion wasGeneratedBy ECO_0000203 NP938256.RAbPeDKZ_un8l0N-6OK_ghCtVPMk1ep62wIUVjtPhv--U130_provenance.
- befree-2016 importedOn "2016-02-19" NP938256.RAbPeDKZ_un8l0N-6OK_ghCtVPMk1ep62wIUVjtPhv--U130_provenance.