Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP401107.RA1u9EWwrfbh51KJwGOT8Zck5gd_WSU5SrQyga_MrzBHQ130_assertion> ?p ?o ?g. }
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- NP401107.RA1u9EWwrfbh51KJwGOT8Zck5gd_WSU5SrQyga_MrzBHQ130_assertion type Assertion NP401107.RA1u9EWwrfbh51KJwGOT8Zck5gd_WSU5SrQyga_MrzBHQ130_head.
- NP401107.RA1u9EWwrfbh51KJwGOT8Zck5gd_WSU5SrQyga_MrzBHQ130_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." NP401107.RA1u9EWwrfbh51KJwGOT8Zck5gd_WSU5SrQyga_MrzBHQ130_provenance.
- NP401107.RA1u9EWwrfbh51KJwGOT8Zck5gd_WSU5SrQyga_MrzBHQ130_assertion evidence source_evidence_literature NP401107.RA1u9EWwrfbh51KJwGOT8Zck5gd_WSU5SrQyga_MrzBHQ130_provenance.
- NP401107.RA1u9EWwrfbh51KJwGOT8Zck5gd_WSU5SrQyga_MrzBHQ130_assertion SIO_000772 16807713 NP401107.RA1u9EWwrfbh51KJwGOT8Zck5gd_WSU5SrQyga_MrzBHQ130_provenance.
- NP401107.RA1u9EWwrfbh51KJwGOT8Zck5gd_WSU5SrQyga_MrzBHQ130_assertion wasDerivedFrom befree-20140225 NP401107.RA1u9EWwrfbh51KJwGOT8Zck5gd_WSU5SrQyga_MrzBHQ130_provenance.
- NP401107.RA1u9EWwrfbh51KJwGOT8Zck5gd_WSU5SrQyga_MrzBHQ130_assertion wasGeneratedBy ECO_0000203 NP401107.RA1u9EWwrfbh51KJwGOT8Zck5gd_WSU5SrQyga_MrzBHQ130_provenance.