Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP422488.RAWmiVr93qGCy2HMvUcgMjKInijvarMerwTA6m04Aue34130_assertion> ?p ?o ?g. }
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- NP422488.RAWmiVr93qGCy2HMvUcgMjKInijvarMerwTA6m04Aue34130_assertion type Assertion NP422488.RAWmiVr93qGCy2HMvUcgMjKInijvarMerwTA6m04Aue34130_head.
- NP422488.RAWmiVr93qGCy2HMvUcgMjKInijvarMerwTA6m04Aue34130_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." NP422488.RAWmiVr93qGCy2HMvUcgMjKInijvarMerwTA6m04Aue34130_provenance.
- NP422488.RAWmiVr93qGCy2HMvUcgMjKInijvarMerwTA6m04Aue34130_assertion evidence source_evidence_literature NP422488.RAWmiVr93qGCy2HMvUcgMjKInijvarMerwTA6m04Aue34130_provenance.
- NP422488.RAWmiVr93qGCy2HMvUcgMjKInijvarMerwTA6m04Aue34130_assertion SIO_000772 16807713 NP422488.RAWmiVr93qGCy2HMvUcgMjKInijvarMerwTA6m04Aue34130_provenance.
- NP422488.RAWmiVr93qGCy2HMvUcgMjKInijvarMerwTA6m04Aue34130_assertion wasDerivedFrom befree-20140225 NP422488.RAWmiVr93qGCy2HMvUcgMjKInijvarMerwTA6m04Aue34130_provenance.
- NP422488.RAWmiVr93qGCy2HMvUcgMjKInijvarMerwTA6m04Aue34130_assertion wasGeneratedBy ECO_0000203 NP422488.RAWmiVr93qGCy2HMvUcgMjKInijvarMerwTA6m04Aue34130_provenance.