Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP224573.RAC_njpUyHsGS7HgyJw7oBwwVXz58ovaeiW7FtVSUdu4M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP224573.RAC_njpUyHsGS7HgyJw7oBwwVXz58ovaeiW7FtVSUdu4M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP224573.RAC_njpUyHsGS7HgyJw7oBwwVXz58ovaeiW7FtVSUdu4M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP224573.RAC_njpUyHsGS7HgyJw7oBwwVXz58ovaeiW7FtVSUdu4M130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP224573.RAC_njpUyHsGS7HgyJw7oBwwVXz58ovaeiW7FtVSUdu4M130_provenance.
- NP224573.RAC_njpUyHsGS7HgyJw7oBwwVXz58ovaeiW7FtVSUdu4M130_assertion wasGeneratedBy ECO_0000203 NP224573.RAC_njpUyHsGS7HgyJw7oBwwVXz58ovaeiW7FtVSUdu4M130_provenance.
- NP224573.RAC_njpUyHsGS7HgyJw7oBwwVXz58ovaeiW7FtVSUdu4M130_assertion wasDerivedFrom lhgdn-20090331 NP224573.RAC_njpUyHsGS7HgyJw7oBwwVXz58ovaeiW7FtVSUdu4M130_provenance.
- NP224573.RAC_njpUyHsGS7HgyJw7oBwwVXz58ovaeiW7FtVSUdu4M130_assertion SIO_000772 17457594 NP224573.RAC_njpUyHsGS7HgyJw7oBwwVXz58ovaeiW7FtVSUdu4M130_provenance.
- NP224573.RAC_njpUyHsGS7HgyJw7oBwwVXz58ovaeiW7FtVSUdu4M130_assertion evidence source_evidence_literature NP224573.RAC_njpUyHsGS7HgyJw7oBwwVXz58ovaeiW7FtVSUdu4M130_provenance.
- NP224573.RAC_njpUyHsGS7HgyJw7oBwwVXz58ovaeiW7FtVSUdu4M130_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." NP224573.RAC_njpUyHsGS7HgyJw7oBwwVXz58ovaeiW7FtVSUdu4M130_provenance.