Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP675448.RA2sXcLNAf6qFN7tEOEoI2BP-ovfkeChs0DFC2u5oEZOA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP675448.RA2sXcLNAf6qFN7tEOEoI2BP-ovfkeChs0DFC2u5oEZOA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP675448.RA2sXcLNAf6qFN7tEOEoI2BP-ovfkeChs0DFC2u5oEZOA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP675448.RA2sXcLNAf6qFN7tEOEoI2BP-ovfkeChs0DFC2u5oEZOA130_provenance.
- NP675448.RA2sXcLNAf6qFN7tEOEoI2BP-ovfkeChs0DFC2u5oEZOA130_assertion description "[Mutations in the NOTCH3 gene cause cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), which is clinically characterised by recurrent ischemic strokes, migraine with aura, psychiatric symptoms, cognitive decline and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP675448.RA2sXcLNAf6qFN7tEOEoI2BP-ovfkeChs0DFC2u5oEZOA130_provenance.
- NP675448.RA2sXcLNAf6qFN7tEOEoI2BP-ovfkeChs0DFC2u5oEZOA130_assertion evidence source_evidence_literature NP675448.RA2sXcLNAf6qFN7tEOEoI2BP-ovfkeChs0DFC2u5oEZOA130_provenance.
- NP675448.RA2sXcLNAf6qFN7tEOEoI2BP-ovfkeChs0DFC2u5oEZOA130_assertion SIO_000772 16807713 NP675448.RA2sXcLNAf6qFN7tEOEoI2BP-ovfkeChs0DFC2u5oEZOA130_provenance.
- NP675448.RA2sXcLNAf6qFN7tEOEoI2BP-ovfkeChs0DFC2u5oEZOA130_assertion wasDerivedFrom befree-20140225 NP675448.RA2sXcLNAf6qFN7tEOEoI2BP-ovfkeChs0DFC2u5oEZOA130_provenance.
- NP675448.RA2sXcLNAf6qFN7tEOEoI2BP-ovfkeChs0DFC2u5oEZOA130_assertion wasGeneratedBy ECO_0000203 NP675448.RA2sXcLNAf6qFN7tEOEoI2BP-ovfkeChs0DFC2u5oEZOA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP675448.RA2sXcLNAf6qFN7tEOEoI2BP-ovfkeChs0DFC2u5oEZOA130_provenance.