Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1238902.RAaSMAkK-ma64zR0HkUKkv0Lb6RYQku-fEIS-vEm0Mdw4130_assertion> ?p ?o ?g. }
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- NP1238902.RAaSMAkK-ma64zR0HkUKkv0Lb6RYQku-fEIS-vEm0Mdw4130_assertion type Assertion NP1238902.RAaSMAkK-ma64zR0HkUKkv0Lb6RYQku-fEIS-vEm0Mdw4130_head.
- NP1238902.RAaSMAkK-ma64zR0HkUKkv0Lb6RYQku-fEIS-vEm0Mdw4130_assertion description "[Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is an inherited small vessel disease caused by mutations of the NOTCH3 gene, which result in degeneration of vascular smooth muscle cells, arteriolar stenosis, and impaired cerebral blood flow.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1238902.RAaSMAkK-ma64zR0HkUKkv0Lb6RYQku-fEIS-vEm0Mdw4130_provenance.
- NP1238902.RAaSMAkK-ma64zR0HkUKkv0Lb6RYQku-fEIS-vEm0Mdw4130_assertion evidence source_evidence_literature NP1238902.RAaSMAkK-ma64zR0HkUKkv0Lb6RYQku-fEIS-vEm0Mdw4130_provenance.
- NP1238902.RAaSMAkK-ma64zR0HkUKkv0Lb6RYQku-fEIS-vEm0Mdw4130_assertion SIO_000772 25412914 NP1238902.RAaSMAkK-ma64zR0HkUKkv0Lb6RYQku-fEIS-vEm0Mdw4130_provenance.
- NP1238902.RAaSMAkK-ma64zR0HkUKkv0Lb6RYQku-fEIS-vEm0Mdw4130_assertion wasDerivedFrom befree-2016 NP1238902.RAaSMAkK-ma64zR0HkUKkv0Lb6RYQku-fEIS-vEm0Mdw4130_provenance.
- NP1238902.RAaSMAkK-ma64zR0HkUKkv0Lb6RYQku-fEIS-vEm0Mdw4130_assertion wasGeneratedBy ECO_0000203 NP1238902.RAaSMAkK-ma64zR0HkUKkv0Lb6RYQku-fEIS-vEm0Mdw4130_provenance.