Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP783299.RAvXA6wLi0KJT9bwolezRXLC4dHPId7Xe6-jFmT0vyAU8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP783299.RAvXA6wLi0KJT9bwolezRXLC4dHPId7Xe6-jFmT0vyAU8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP783299.RAvXA6wLi0KJT9bwolezRXLC4dHPId7Xe6-jFmT0vyAU8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP783299.RAvXA6wLi0KJT9bwolezRXLC4dHPId7Xe6-jFmT0vyAU8130_provenance.
- NP783299.RAvXA6wLi0KJT9bwolezRXLC4dHPId7Xe6-jFmT0vyAU8130_assertion description "[Inclusion body myopathy with Paget's disease of bone and frontotemporal dementia (IBMPFD) is caused by mutations in Valosin-containing protein (VCP), a hexameric AAA ATPase that participates in a variety of cellular processes such as protein degradation, organelle biogenesis, and cell-cycle regulation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP783299.RAvXA6wLi0KJT9bwolezRXLC4dHPId7Xe6-jFmT0vyAU8130_provenance.
- NP783299.RAvXA6wLi0KJT9bwolezRXLC4dHPId7Xe6-jFmT0vyAU8130_assertion evidence source_evidence_literature NP783299.RAvXA6wLi0KJT9bwolezRXLC4dHPId7Xe6-jFmT0vyAU8130_provenance.
- NP783299.RAvXA6wLi0KJT9bwolezRXLC4dHPId7Xe6-jFmT0vyAU8130_assertion SIO_000772 21304887 NP783299.RAvXA6wLi0KJT9bwolezRXLC4dHPId7Xe6-jFmT0vyAU8130_provenance.
- NP783299.RAvXA6wLi0KJT9bwolezRXLC4dHPId7Xe6-jFmT0vyAU8130_assertion wasDerivedFrom befree-20140225 NP783299.RAvXA6wLi0KJT9bwolezRXLC4dHPId7Xe6-jFmT0vyAU8130_provenance.
- NP783299.RAvXA6wLi0KJT9bwolezRXLC4dHPId7Xe6-jFmT0vyAU8130_assertion wasGeneratedBy ECO_0000203 NP783299.RAvXA6wLi0KJT9bwolezRXLC4dHPId7Xe6-jFmT0vyAU8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP783299.RAvXA6wLi0KJT9bwolezRXLC4dHPId7Xe6-jFmT0vyAU8130_provenance.