Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP315833.RA8K0h4u1rCqKp2jl3XoU8N2evyLplzkxDZaDXtJBJB5s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP315833.RA8K0h4u1rCqKp2jl3XoU8N2evyLplzkxDZaDXtJBJB5s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP315833.RA8K0h4u1rCqKp2jl3XoU8N2evyLplzkxDZaDXtJBJB5s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP315833.RA8K0h4u1rCqKp2jl3XoU8N2evyLplzkxDZaDXtJBJB5s130_provenance.
- NP315833.RA8K0h4u1rCqKp2jl3XoU8N2evyLplzkxDZaDXtJBJB5s130_assertion wasGeneratedBy ECO_0000203 NP315833.RA8K0h4u1rCqKp2jl3XoU8N2evyLplzkxDZaDXtJBJB5s130_provenance.
- NP315833.RA8K0h4u1rCqKp2jl3XoU8N2evyLplzkxDZaDXtJBJB5s130_assertion wasDerivedFrom befree-20140225 NP315833.RA8K0h4u1rCqKp2jl3XoU8N2evyLplzkxDZaDXtJBJB5s130_provenance.
- NP315833.RA8K0h4u1rCqKp2jl3XoU8N2evyLplzkxDZaDXtJBJB5s130_assertion SIO_000772 17457594 NP315833.RA8K0h4u1rCqKp2jl3XoU8N2evyLplzkxDZaDXtJBJB5s130_provenance.
- NP315833.RA8K0h4u1rCqKp2jl3XoU8N2evyLplzkxDZaDXtJBJB5s130_assertion evidence source_evidence_literature NP315833.RA8K0h4u1rCqKp2jl3XoU8N2evyLplzkxDZaDXtJBJB5s130_provenance.
- NP315833.RA8K0h4u1rCqKp2jl3XoU8N2evyLplzkxDZaDXtJBJB5s130_assertion description "[Frontotemporal dementia with inclusion body myopathy and Paget's disease of bone (IBMPFD) is a rare, autosomal dominant disorder caused by mutations in the gene valosin-containing protein (VCP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP315833.RA8K0h4u1rCqKp2jl3XoU8N2evyLplzkxDZaDXtJBJB5s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP315833.RA8K0h4u1rCqKp2jl3XoU8N2evyLplzkxDZaDXtJBJB5s130_provenance.