Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP557223.RAHloPDHP8La9nkMKnLSiT5S-AvN34i39hofOpVJ7fPa8130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP557223.RAHloPDHP8La9nkMKnLSiT5S-AvN34i39hofOpVJ7fPa8130_assertion type Assertion NP557223.RAHloPDHP8La9nkMKnLSiT5S-AvN34i39hofOpVJ7fPa8130_head.
- NP557223.RAHloPDHP8La9nkMKnLSiT5S-AvN34i39hofOpVJ7fPa8130_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." NP557223.RAHloPDHP8La9nkMKnLSiT5S-AvN34i39hofOpVJ7fPa8130_provenance.
- NP557223.RAHloPDHP8La9nkMKnLSiT5S-AvN34i39hofOpVJ7fPa8130_assertion evidence source_evidence_literature NP557223.RAHloPDHP8La9nkMKnLSiT5S-AvN34i39hofOpVJ7fPa8130_provenance.
- NP557223.RAHloPDHP8La9nkMKnLSiT5S-AvN34i39hofOpVJ7fPa8130_assertion SIO_000772 16807713 NP557223.RAHloPDHP8La9nkMKnLSiT5S-AvN34i39hofOpVJ7fPa8130_provenance.
- NP557223.RAHloPDHP8La9nkMKnLSiT5S-AvN34i39hofOpVJ7fPa8130_assertion wasDerivedFrom befree-2016 NP557223.RAHloPDHP8La9nkMKnLSiT5S-AvN34i39hofOpVJ7fPa8130_provenance.
- NP557223.RAHloPDHP8La9nkMKnLSiT5S-AvN34i39hofOpVJ7fPa8130_assertion wasGeneratedBy ECO_0000203 NP557223.RAHloPDHP8La9nkMKnLSiT5S-AvN34i39hofOpVJ7fPa8130_provenance.