Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- 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.