Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP776604.RAit3SKdA-f9nUmW7GbbYyU1Uobo4x1q69E0CYaCHVSPo130_assertion> ?p ?o ?g. }
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- NP776604.RAit3SKdA-f9nUmW7GbbYyU1Uobo4x1q69E0CYaCHVSPo130_assertion type Assertion NP776604.RAit3SKdA-f9nUmW7GbbYyU1Uobo4x1q69E0CYaCHVSPo130_head.
- NP776604.RAit3SKdA-f9nUmW7GbbYyU1Uobo4x1q69E0CYaCHVSPo130_assertion wasGeneratedBy ECO_0000203 NP776604.RAit3SKdA-f9nUmW7GbbYyU1Uobo4x1q69E0CYaCHVSPo130_provenance.
- NP776604.RAit3SKdA-f9nUmW7GbbYyU1Uobo4x1q69E0CYaCHVSPo130_assertion wasDerivedFrom befree-2016 NP776604.RAit3SKdA-f9nUmW7GbbYyU1Uobo4x1q69E0CYaCHVSPo130_provenance.
- NP776604.RAit3SKdA-f9nUmW7GbbYyU1Uobo4x1q69E0CYaCHVSPo130_assertion SIO_000772 19923742 NP776604.RAit3SKdA-f9nUmW7GbbYyU1Uobo4x1q69E0CYaCHVSPo130_provenance.
- NP776604.RAit3SKdA-f9nUmW7GbbYyU1Uobo4x1q69E0CYaCHVSPo130_assertion evidence source_evidence_literature NP776604.RAit3SKdA-f9nUmW7GbbYyU1Uobo4x1q69E0CYaCHVSPo130_provenance.
- NP776604.RAit3SKdA-f9nUmW7GbbYyU1Uobo4x1q69E0CYaCHVSPo130_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." NP776604.RAit3SKdA-f9nUmW7GbbYyU1Uobo4x1q69E0CYaCHVSPo130_provenance.