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- source_evidence_literature type ECO_0000212 NP570122.RAQDJ-PwR2vc2ONK3WslOkH-mi474PxXs3fNc5Hz5afjA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP570122.RAQDJ-PwR2vc2ONK3WslOkH-mi474PxXs3fNc5Hz5afjA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP570122.RAQDJ-PwR2vc2ONK3WslOkH-mi474PxXs3fNc5Hz5afjA130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP570122.RAQDJ-PwR2vc2ONK3WslOkH-mi474PxXs3fNc5Hz5afjA130_provenance.