Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP570122.RAQDJ-PwR2vc2ONK3WslOkH-mi474PxXs3fNc5Hz5afjA130_assertion> ?p ?o ?g. }
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- NP570122.RAQDJ-PwR2vc2ONK3WslOkH-mi474PxXs3fNc5Hz5afjA130_assertion type Assertion NP570122.RAQDJ-PwR2vc2ONK3WslOkH-mi474PxXs3fNc5Hz5afjA130_head.
- NP570122.RAQDJ-PwR2vc2ONK3WslOkH-mi474PxXs3fNc5Hz5afjA130_assertion description "[Mutations in the valosin-containing protein (VCP, p97) gene on chromosome 9p13-p12 cause a late-onset form of autosomal dominant inclusion body myopathy associated with Paget disease of the bone and frontotemporal dementia (IBMPFD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP570122.RAQDJ-PwR2vc2ONK3WslOkH-mi474PxXs3fNc5Hz5afjA130_provenance.
- NP570122.RAQDJ-PwR2vc2ONK3WslOkH-mi474PxXs3fNc5Hz5afjA130_assertion evidence source_evidence_literature NP570122.RAQDJ-PwR2vc2ONK3WslOkH-mi474PxXs3fNc5Hz5afjA130_provenance.
- NP570122.RAQDJ-PwR2vc2ONK3WslOkH-mi474PxXs3fNc5Hz5afjA130_assertion SIO_000772 16984901 NP570122.RAQDJ-PwR2vc2ONK3WslOkH-mi474PxXs3fNc5Hz5afjA130_provenance.
- NP570122.RAQDJ-PwR2vc2ONK3WslOkH-mi474PxXs3fNc5Hz5afjA130_assertion wasDerivedFrom befree-2016 NP570122.RAQDJ-PwR2vc2ONK3WslOkH-mi474PxXs3fNc5Hz5afjA130_provenance.
- NP570122.RAQDJ-PwR2vc2ONK3WslOkH-mi474PxXs3fNc5Hz5afjA130_assertion wasGeneratedBy ECO_0000203 NP570122.RAQDJ-PwR2vc2ONK3WslOkH-mi474PxXs3fNc5Hz5afjA130_provenance.