Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP556039.RAAo14NuoLTKNz2rxcGq_iY0iBKvKcO-UtWv74UVHAjvg130_assertion> ?p ?o ?g. }
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- NP556039.RAAo14NuoLTKNz2rxcGq_iY0iBKvKcO-UtWv74UVHAjvg130_assertion type Assertion NP556039.RAAo14NuoLTKNz2rxcGq_iY0iBKvKcO-UtWv74UVHAjvg130_head.
- NP556039.RAAo14NuoLTKNz2rxcGq_iY0iBKvKcO-UtWv74UVHAjvg130_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." NP556039.RAAo14NuoLTKNz2rxcGq_iY0iBKvKcO-UtWv74UVHAjvg130_provenance.
- NP556039.RAAo14NuoLTKNz2rxcGq_iY0iBKvKcO-UtWv74UVHAjvg130_assertion evidence source_evidence_literature NP556039.RAAo14NuoLTKNz2rxcGq_iY0iBKvKcO-UtWv74UVHAjvg130_provenance.
- NP556039.RAAo14NuoLTKNz2rxcGq_iY0iBKvKcO-UtWv74UVHAjvg130_assertion SIO_000772 16807713 NP556039.RAAo14NuoLTKNz2rxcGq_iY0iBKvKcO-UtWv74UVHAjvg130_provenance.
- NP556039.RAAo14NuoLTKNz2rxcGq_iY0iBKvKcO-UtWv74UVHAjvg130_assertion wasDerivedFrom befree-20140225 NP556039.RAAo14NuoLTKNz2rxcGq_iY0iBKvKcO-UtWv74UVHAjvg130_provenance.
- NP556039.RAAo14NuoLTKNz2rxcGq_iY0iBKvKcO-UtWv74UVHAjvg130_assertion wasGeneratedBy ECO_0000203 NP556039.RAAo14NuoLTKNz2rxcGq_iY0iBKvKcO-UtWv74UVHAjvg130_provenance.