Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP385655.RAgr1Z_sFaAA0Kzo3TyWT3tcuz5_U-WgPtFQllgsczNqo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP385655.RAgr1Z_sFaAA0Kzo3TyWT3tcuz5_U-WgPtFQllgsczNqo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP385655.RAgr1Z_sFaAA0Kzo3TyWT3tcuz5_U-WgPtFQllgsczNqo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP385655.RAgr1Z_sFaAA0Kzo3TyWT3tcuz5_U-WgPtFQllgsczNqo130_provenance.
- NP385655.RAgr1Z_sFaAA0Kzo3TyWT3tcuz5_U-WgPtFQllgsczNqo130_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." NP385655.RAgr1Z_sFaAA0Kzo3TyWT3tcuz5_U-WgPtFQllgsczNqo130_provenance.
- NP385655.RAgr1Z_sFaAA0Kzo3TyWT3tcuz5_U-WgPtFQllgsczNqo130_assertion evidence source_evidence_literature NP385655.RAgr1Z_sFaAA0Kzo3TyWT3tcuz5_U-WgPtFQllgsczNqo130_provenance.
- NP385655.RAgr1Z_sFaAA0Kzo3TyWT3tcuz5_U-WgPtFQllgsczNqo130_assertion SIO_000772 22078486 NP385655.RAgr1Z_sFaAA0Kzo3TyWT3tcuz5_U-WgPtFQllgsczNqo130_provenance.
- NP385655.RAgr1Z_sFaAA0Kzo3TyWT3tcuz5_U-WgPtFQllgsczNqo130_assertion wasDerivedFrom befree-20140225 NP385655.RAgr1Z_sFaAA0Kzo3TyWT3tcuz5_U-WgPtFQllgsczNqo130_provenance.
- NP385655.RAgr1Z_sFaAA0Kzo3TyWT3tcuz5_U-WgPtFQllgsczNqo130_assertion wasGeneratedBy ECO_0000203 NP385655.RAgr1Z_sFaAA0Kzo3TyWT3tcuz5_U-WgPtFQllgsczNqo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP385655.RAgr1Z_sFaAA0Kzo3TyWT3tcuz5_U-WgPtFQllgsczNqo130_provenance.