Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP783976.RACMhXogcEqBtA_CffMT0d0CQd09KOQyIpxNPDs3-_ofU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP783976.RACMhXogcEqBtA_CffMT0d0CQd09KOQyIpxNPDs3-_ofU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP783976.RACMhXogcEqBtA_CffMT0d0CQd09KOQyIpxNPDs3-_ofU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP783976.RACMhXogcEqBtA_CffMT0d0CQd09KOQyIpxNPDs3-_ofU130_provenance.
- befree-2016 importedOn "2016-02-19" NP783976.RACMhXogcEqBtA_CffMT0d0CQd09KOQyIpxNPDs3-_ofU130_provenance.
- NP783976.RACMhXogcEqBtA_CffMT0d0CQd09KOQyIpxNPDs3-_ofU130_assertion wasGeneratedBy ECO_0000203 NP783976.RACMhXogcEqBtA_CffMT0d0CQd09KOQyIpxNPDs3-_ofU130_provenance.
- NP783976.RACMhXogcEqBtA_CffMT0d0CQd09KOQyIpxNPDs3-_ofU130_assertion wasDerivedFrom befree-2016 NP783976.RACMhXogcEqBtA_CffMT0d0CQd09KOQyIpxNPDs3-_ofU130_provenance.
- NP783976.RACMhXogcEqBtA_CffMT0d0CQd09KOQyIpxNPDs3-_ofU130_assertion SIO_000772 20038773 NP783976.RACMhXogcEqBtA_CffMT0d0CQd09KOQyIpxNPDs3-_ofU130_provenance.
- NP783976.RACMhXogcEqBtA_CffMT0d0CQd09KOQyIpxNPDs3-_ofU130_assertion evidence source_evidence_literature NP783976.RACMhXogcEqBtA_CffMT0d0CQd09KOQyIpxNPDs3-_ofU130_provenance.
- NP783976.RACMhXogcEqBtA_CffMT0d0CQd09KOQyIpxNPDs3-_ofU130_assertion description "[Some features were significantly (Fisher exact test p < 0.05) more frequent in CADASIL than in NOTCH3-negative patients: history of migraine (73 vs 39%), stroke before the age of 60 among relatives (71 vs 32%), severe leukoencephalopathy (94 vs 62%), white matter changes extended to the anterior temporal lobes (93 vs 45%), external capsule involvement (100 vs 50%), and presence of lacunar infarcts (100 vs 65%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP783976.RACMhXogcEqBtA_CffMT0d0CQd09KOQyIpxNPDs3-_ofU130_provenance.