Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP564838.RAh8bvT1P2r4Sa6EXZe0b-mFmvNzExXR41QBw2bNQnmBY130_assertion> ?p ?o ?g. }
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- NP564838.RAh8bvT1P2r4Sa6EXZe0b-mFmvNzExXR41QBw2bNQnmBY130_assertion type Assertion NP564838.RAh8bvT1P2r4Sa6EXZe0b-mFmvNzExXR41QBw2bNQnmBY130_head.
- NP564838.RAh8bvT1P2r4Sa6EXZe0b-mFmvNzExXR41QBw2bNQnmBY130_assertion description "[Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a heritable small-vessel disease caused by mutations in NOTCH3 gene and clinically characterized 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." NP564838.RAh8bvT1P2r4Sa6EXZe0b-mFmvNzExXR41QBw2bNQnmBY130_provenance.
- NP564838.RAh8bvT1P2r4Sa6EXZe0b-mFmvNzExXR41QBw2bNQnmBY130_assertion evidence source_evidence_literature NP564838.RAh8bvT1P2r4Sa6EXZe0b-mFmvNzExXR41QBw2bNQnmBY130_provenance.
- NP564838.RAh8bvT1P2r4Sa6EXZe0b-mFmvNzExXR41QBw2bNQnmBY130_assertion SIO_000772 19576955 NP564838.RAh8bvT1P2r4Sa6EXZe0b-mFmvNzExXR41QBw2bNQnmBY130_provenance.
- NP564838.RAh8bvT1P2r4Sa6EXZe0b-mFmvNzExXR41QBw2bNQnmBY130_assertion wasDerivedFrom befree-20140225 NP564838.RAh8bvT1P2r4Sa6EXZe0b-mFmvNzExXR41QBw2bNQnmBY130_provenance.
- NP564838.RAh8bvT1P2r4Sa6EXZe0b-mFmvNzExXR41QBw2bNQnmBY130_assertion wasGeneratedBy ECO_0000203 NP564838.RAh8bvT1P2r4Sa6EXZe0b-mFmvNzExXR41QBw2bNQnmBY130_provenance.