Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP586132.RAaTJye1VPsu4z94V3-swI_1Lupig76yCxWrT5OWWcYDU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP586132.RAaTJye1VPsu4z94V3-swI_1Lupig76yCxWrT5OWWcYDU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP586132.RAaTJye1VPsu4z94V3-swI_1Lupig76yCxWrT5OWWcYDU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP586132.RAaTJye1VPsu4z94V3-swI_1Lupig76yCxWrT5OWWcYDU130_provenance.
- NP586132.RAaTJye1VPsu4z94V3-swI_1Lupig76yCxWrT5OWWcYDU130_assertion wasGeneratedBy ECO_0000203 NP586132.RAaTJye1VPsu4z94V3-swI_1Lupig76yCxWrT5OWWcYDU130_provenance.
- NP586132.RAaTJye1VPsu4z94V3-swI_1Lupig76yCxWrT5OWWcYDU130_assertion wasDerivedFrom befree-20140225 NP586132.RAaTJye1VPsu4z94V3-swI_1Lupig76yCxWrT5OWWcYDU130_provenance.
- NP586132.RAaTJye1VPsu4z94V3-swI_1Lupig76yCxWrT5OWWcYDU130_assertion SIO_000772 11755616 NP586132.RAaTJye1VPsu4z94V3-swI_1Lupig76yCxWrT5OWWcYDU130_provenance.
- NP586132.RAaTJye1VPsu4z94V3-swI_1Lupig76yCxWrT5OWWcYDU130_assertion evidence source_evidence_literature NP586132.RAaTJye1VPsu4z94V3-swI_1Lupig76yCxWrT5OWWcYDU130_provenance.
- NP586132.RAaTJye1VPsu4z94V3-swI_1Lupig76yCxWrT5OWWcYDU130_assertion description "[CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy) is a small-artery disease of the brain caused by NOTCH3 mutations that lead to an abnormal accumulation of NOTCH3 within the vasculature.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP586132.RAaTJye1VPsu4z94V3-swI_1Lupig76yCxWrT5OWWcYDU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP586132.RAaTJye1VPsu4z94V3-swI_1Lupig76yCxWrT5OWWcYDU130_provenance.