Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP596598.RAaWAPUZCEvjd9oO3gTStgvh6hBRb3NBb0cEK8CeJY-2s130_assertion> ?p ?o ?g. }
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- NP596598.RAaWAPUZCEvjd9oO3gTStgvh6hBRb3NBb0cEK8CeJY-2s130_assertion type Assertion NP596598.RAaWAPUZCEvjd9oO3gTStgvh6hBRb3NBb0cEK8CeJY-2s130_head.
- NP596598.RAaWAPUZCEvjd9oO3gTStgvh6hBRb3NBb0cEK8CeJY-2s130_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." NP596598.RAaWAPUZCEvjd9oO3gTStgvh6hBRb3NBb0cEK8CeJY-2s130_provenance.
- NP596598.RAaWAPUZCEvjd9oO3gTStgvh6hBRb3NBb0cEK8CeJY-2s130_assertion evidence source_evidence_literature NP596598.RAaWAPUZCEvjd9oO3gTStgvh6hBRb3NBb0cEK8CeJY-2s130_provenance.
- NP596598.RAaWAPUZCEvjd9oO3gTStgvh6hBRb3NBb0cEK8CeJY-2s130_assertion SIO_000772 16807713 NP596598.RAaWAPUZCEvjd9oO3gTStgvh6hBRb3NBb0cEK8CeJY-2s130_provenance.
- NP596598.RAaWAPUZCEvjd9oO3gTStgvh6hBRb3NBb0cEK8CeJY-2s130_assertion wasDerivedFrom befree-20150227 NP596598.RAaWAPUZCEvjd9oO3gTStgvh6hBRb3NBb0cEK8CeJY-2s130_provenance.
- NP596598.RAaWAPUZCEvjd9oO3gTStgvh6hBRb3NBb0cEK8CeJY-2s130_assertion wasGeneratedBy ECO_0000203 NP596598.RAaWAPUZCEvjd9oO3gTStgvh6hBRb3NBb0cEK8CeJY-2s130_provenance.