Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP768987.RAgYkNKpBmjKgCPOGoPwbRVxdjc9Zv5bUw7yz1VEiIHoc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP768987.RAgYkNKpBmjKgCPOGoPwbRVxdjc9Zv5bUw7yz1VEiIHoc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP768987.RAgYkNKpBmjKgCPOGoPwbRVxdjc9Zv5bUw7yz1VEiIHoc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP768987.RAgYkNKpBmjKgCPOGoPwbRVxdjc9Zv5bUw7yz1VEiIHoc130_provenance.
- NP768987.RAgYkNKpBmjKgCPOGoPwbRVxdjc9Zv5bUw7yz1VEiIHoc130_assertion description "[Mutations in the valosin-containing protein (VCP) gene on chromosome 9p13-p12 recently have been shown to cause autosomal dominant inclusion body myopathy associated with Paget's disease of the bone and frontotemporal dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768987.RAgYkNKpBmjKgCPOGoPwbRVxdjc9Zv5bUw7yz1VEiIHoc130_provenance.
- NP768987.RAgYkNKpBmjKgCPOGoPwbRVxdjc9Zv5bUw7yz1VEiIHoc130_assertion evidence source_evidence_literature NP768987.RAgYkNKpBmjKgCPOGoPwbRVxdjc9Zv5bUw7yz1VEiIHoc130_provenance.
- NP768987.RAgYkNKpBmjKgCPOGoPwbRVxdjc9Zv5bUw7yz1VEiIHoc130_assertion SIO_000772 15732117 NP768987.RAgYkNKpBmjKgCPOGoPwbRVxdjc9Zv5bUw7yz1VEiIHoc130_provenance.
- NP768987.RAgYkNKpBmjKgCPOGoPwbRVxdjc9Zv5bUw7yz1VEiIHoc130_assertion wasDerivedFrom befree-20150227 NP768987.RAgYkNKpBmjKgCPOGoPwbRVxdjc9Zv5bUw7yz1VEiIHoc130_provenance.
- NP768987.RAgYkNKpBmjKgCPOGoPwbRVxdjc9Zv5bUw7yz1VEiIHoc130_assertion wasGeneratedBy ECO_0000203 NP768987.RAgYkNKpBmjKgCPOGoPwbRVxdjc9Zv5bUw7yz1VEiIHoc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP768987.RAgYkNKpBmjKgCPOGoPwbRVxdjc9Zv5bUw7yz1VEiIHoc130_provenance.