Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP898195.RA9oSuz77wPjLf0K8L5YpmB16VQekJI3kPR2ItLiM1AIk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP898195.RA9oSuz77wPjLf0K8L5YpmB16VQekJI3kPR2ItLiM1AIk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP898195.RA9oSuz77wPjLf0K8L5YpmB16VQekJI3kPR2ItLiM1AIk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP898195.RA9oSuz77wPjLf0K8L5YpmB16VQekJI3kPR2ItLiM1AIk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP898195.RA9oSuz77wPjLf0K8L5YpmB16VQekJI3kPR2ItLiM1AIk130_provenance.
- NP898195.RA9oSuz77wPjLf0K8L5YpmB16VQekJI3kPR2ItLiM1AIk130_assertion wasGeneratedBy ECO_0000203 NP898195.RA9oSuz77wPjLf0K8L5YpmB16VQekJI3kPR2ItLiM1AIk130_provenance.
- NP898195.RA9oSuz77wPjLf0K8L5YpmB16VQekJI3kPR2ItLiM1AIk130_assertion wasDerivedFrom befree-20150227 NP898195.RA9oSuz77wPjLf0K8L5YpmB16VQekJI3kPR2ItLiM1AIk130_provenance.
- NP898195.RA9oSuz77wPjLf0K8L5YpmB16VQekJI3kPR2ItLiM1AIk130_assertion SIO_000772 19923742 NP898195.RA9oSuz77wPjLf0K8L5YpmB16VQekJI3kPR2ItLiM1AIk130_provenance.
- NP898195.RA9oSuz77wPjLf0K8L5YpmB16VQekJI3kPR2ItLiM1AIk130_assertion evidence source_evidence_literature NP898195.RA9oSuz77wPjLf0K8L5YpmB16VQekJI3kPR2ItLiM1AIk130_provenance.
- NP898195.RA9oSuz77wPjLf0K8L5YpmB16VQekJI3kPR2ItLiM1AIk130_assertion description "[Mutations in p97 have been implicated in patients with inclusion-body myopathy associated with Paget's disease of the bone and frontotemporal dementia (IBMPFD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP898195.RA9oSuz77wPjLf0K8L5YpmB16VQekJI3kPR2ItLiM1AIk130_provenance.