Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP768791.RA2wPUXEJEV5a-QgJ31o1Y_gTtgNU81dduCB1RbGA7PWA130_assertion> ?p ?o ?g. }
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- NP768791.RA2wPUXEJEV5a-QgJ31o1Y_gTtgNU81dduCB1RbGA7PWA130_assertion type Assertion NP768791.RA2wPUXEJEV5a-QgJ31o1Y_gTtgNU81dduCB1RbGA7PWA130_head.
- NP768791.RA2wPUXEJEV5a-QgJ31o1Y_gTtgNU81dduCB1RbGA7PWA130_assertion description "[A genetic deficiency of VCP can cause inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia (IBMPFD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768791.RA2wPUXEJEV5a-QgJ31o1Y_gTtgNU81dduCB1RbGA7PWA130_provenance.
- NP768791.RA2wPUXEJEV5a-QgJ31o1Y_gTtgNU81dduCB1RbGA7PWA130_assertion evidence source_evidence_literature NP768791.RA2wPUXEJEV5a-QgJ31o1Y_gTtgNU81dduCB1RbGA7PWA130_provenance.
- NP768791.RA2wPUXEJEV5a-QgJ31o1Y_gTtgNU81dduCB1RbGA7PWA130_assertion SIO_000772 25447673 NP768791.RA2wPUXEJEV5a-QgJ31o1Y_gTtgNU81dduCB1RbGA7PWA130_provenance.
- NP768791.RA2wPUXEJEV5a-QgJ31o1Y_gTtgNU81dduCB1RbGA7PWA130_assertion wasDerivedFrom befree-20150227 NP768791.RA2wPUXEJEV5a-QgJ31o1Y_gTtgNU81dduCB1RbGA7PWA130_provenance.
- NP768791.RA2wPUXEJEV5a-QgJ31o1Y_gTtgNU81dduCB1RbGA7PWA130_assertion wasGeneratedBy ECO_0000203 NP768791.RA2wPUXEJEV5a-QgJ31o1Y_gTtgNU81dduCB1RbGA7PWA130_provenance.