Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP436368.RA_uTLnxiOsjaG3loETVXewavRl6JJJk6W0IZMvJVcJwU130_assertion> ?p ?o ?g. }
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- NP436368.RA_uTLnxiOsjaG3loETVXewavRl6JJJk6W0IZMvJVcJwU130_assertion type Assertion NP436368.RA_uTLnxiOsjaG3loETVXewavRl6JJJk6W0IZMvJVcJwU130_head.
- NP436368.RA_uTLnxiOsjaG3loETVXewavRl6JJJk6W0IZMvJVcJwU130_assertion description "[Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a heritable small-vessel disease caused by mutations in NOTCH3 gene and clinically characterized 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." NP436368.RA_uTLnxiOsjaG3loETVXewavRl6JJJk6W0IZMvJVcJwU130_provenance.
- NP436368.RA_uTLnxiOsjaG3loETVXewavRl6JJJk6W0IZMvJVcJwU130_assertion evidence source_evidence_literature NP436368.RA_uTLnxiOsjaG3loETVXewavRl6JJJk6W0IZMvJVcJwU130_provenance.
- NP436368.RA_uTLnxiOsjaG3loETVXewavRl6JJJk6W0IZMvJVcJwU130_assertion SIO_000772 19576955 NP436368.RA_uTLnxiOsjaG3loETVXewavRl6JJJk6W0IZMvJVcJwU130_provenance.
- NP436368.RA_uTLnxiOsjaG3loETVXewavRl6JJJk6W0IZMvJVcJwU130_assertion wasDerivedFrom befree-20140225 NP436368.RA_uTLnxiOsjaG3loETVXewavRl6JJJk6W0IZMvJVcJwU130_provenance.
- NP436368.RA_uTLnxiOsjaG3loETVXewavRl6JJJk6W0IZMvJVcJwU130_assertion wasGeneratedBy ECO_0000203 NP436368.RA_uTLnxiOsjaG3loETVXewavRl6JJJk6W0IZMvJVcJwU130_provenance.