Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP557224.RAan7MxulkbzeuEvWHYm85rKTJRd0s31NJoDe2GQNs4Vw130_assertion> ?p ?o ?g. }
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- NP557224.RAan7MxulkbzeuEvWHYm85rKTJRd0s31NJoDe2GQNs4Vw130_assertion type Assertion NP557224.RAan7MxulkbzeuEvWHYm85rKTJRd0s31NJoDe2GQNs4Vw130_head.
- NP557224.RAan7MxulkbzeuEvWHYm85rKTJRd0s31NJoDe2GQNs4Vw130_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." NP557224.RAan7MxulkbzeuEvWHYm85rKTJRd0s31NJoDe2GQNs4Vw130_provenance.
- NP557224.RAan7MxulkbzeuEvWHYm85rKTJRd0s31NJoDe2GQNs4Vw130_assertion evidence source_evidence_literature NP557224.RAan7MxulkbzeuEvWHYm85rKTJRd0s31NJoDe2GQNs4Vw130_provenance.
- NP557224.RAan7MxulkbzeuEvWHYm85rKTJRd0s31NJoDe2GQNs4Vw130_assertion SIO_000772 16807713 NP557224.RAan7MxulkbzeuEvWHYm85rKTJRd0s31NJoDe2GQNs4Vw130_provenance.
- NP557224.RAan7MxulkbzeuEvWHYm85rKTJRd0s31NJoDe2GQNs4Vw130_assertion wasDerivedFrom befree-2016 NP557224.RAan7MxulkbzeuEvWHYm85rKTJRd0s31NJoDe2GQNs4Vw130_provenance.
- NP557224.RAan7MxulkbzeuEvWHYm85rKTJRd0s31NJoDe2GQNs4Vw130_assertion wasGeneratedBy ECO_0000203 NP557224.RAan7MxulkbzeuEvWHYm85rKTJRd0s31NJoDe2GQNs4Vw130_provenance.