Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP592371.RA4XcN95AveAr5BOe0LD7t2Fskua86OZAv2gPZECLwQpA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP592371.RA4XcN95AveAr5BOe0LD7t2Fskua86OZAv2gPZECLwQpA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP592371.RA4XcN95AveAr5BOe0LD7t2Fskua86OZAv2gPZECLwQpA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP592371.RA4XcN95AveAr5BOe0LD7t2Fskua86OZAv2gPZECLwQpA130_provenance.
- NP592371.RA4XcN95AveAr5BOe0LD7t2Fskua86OZAv2gPZECLwQpA130_assertion description "[The CNS pathology is characterized by a novel pattern of ubiquitin pathology distinct from sporadic and familial frontotemporal lobar degeneration with ubiquitin-positive inclusions (FTLD-U) without VCP mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP592371.RA4XcN95AveAr5BOe0LD7t2Fskua86OZAv2gPZECLwQpA130_provenance.
- NP592371.RA4XcN95AveAr5BOe0LD7t2Fskua86OZAv2gPZECLwQpA130_assertion evidence source_evidence_literature NP592371.RA4XcN95AveAr5BOe0LD7t2Fskua86OZAv2gPZECLwQpA130_provenance.
- NP592371.RA4XcN95AveAr5BOe0LD7t2Fskua86OZAv2gPZECLwQpA130_assertion SIO_000772 17279000 NP592371.RA4XcN95AveAr5BOe0LD7t2Fskua86OZAv2gPZECLwQpA130_provenance.
- NP592371.RA4XcN95AveAr5BOe0LD7t2Fskua86OZAv2gPZECLwQpA130_assertion wasDerivedFrom befree-2016 NP592371.RA4XcN95AveAr5BOe0LD7t2Fskua86OZAv2gPZECLwQpA130_provenance.
- NP592371.RA4XcN95AveAr5BOe0LD7t2Fskua86OZAv2gPZECLwQpA130_assertion wasGeneratedBy ECO_0000203 NP592371.RA4XcN95AveAr5BOe0LD7t2Fskua86OZAv2gPZECLwQpA130_provenance.
- befree-2016 importedOn "2016-02-19" NP592371.RA4XcN95AveAr5BOe0LD7t2Fskua86OZAv2gPZECLwQpA130_provenance.