Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP246807.RAviPEdMcyt8B6EOzqQlLKscqQ164LKCTXMJLYSh1VtFg130_assertion> ?p ?o ?g. }
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- NP246807.RAviPEdMcyt8B6EOzqQlLKscqQ164LKCTXMJLYSh1VtFg130_assertion type Assertion NP246807.RAviPEdMcyt8B6EOzqQlLKscqQ164LKCTXMJLYSh1VtFg130_head.
- NP246807.RAviPEdMcyt8B6EOzqQlLKscqQ164LKCTXMJLYSh1VtFg130_assertion wasGeneratedBy ECO_0000203 NP246807.RAviPEdMcyt8B6EOzqQlLKscqQ164LKCTXMJLYSh1VtFg130_provenance.
- NP246807.RAviPEdMcyt8B6EOzqQlLKscqQ164LKCTXMJLYSh1VtFg130_assertion wasDerivedFrom befree-20140225 NP246807.RAviPEdMcyt8B6EOzqQlLKscqQ164LKCTXMJLYSh1VtFg130_provenance.
- NP246807.RAviPEdMcyt8B6EOzqQlLKscqQ164LKCTXMJLYSh1VtFg130_assertion SIO_000772 11755616 NP246807.RAviPEdMcyt8B6EOzqQlLKscqQ164LKCTXMJLYSh1VtFg130_provenance.
- NP246807.RAviPEdMcyt8B6EOzqQlLKscqQ164LKCTXMJLYSh1VtFg130_assertion evidence source_evidence_literature NP246807.RAviPEdMcyt8B6EOzqQlLKscqQ164LKCTXMJLYSh1VtFg130_provenance.
- NP246807.RAviPEdMcyt8B6EOzqQlLKscqQ164LKCTXMJLYSh1VtFg130_assertion description "[CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy) is a small-artery disease of the brain caused by NOTCH3 mutations that lead to an abnormal accumulation of NOTCH3 within the vasculature.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP246807.RAviPEdMcyt8B6EOzqQlLKscqQ164LKCTXMJLYSh1VtFg130_provenance.