Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP557225.RASFiyeJpR0polxAple67NNzvpBj7pUZyifunIG8eHJ48130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP557225.RASFiyeJpR0polxAple67NNzvpBj7pUZyifunIG8eHJ48130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP557225.RASFiyeJpR0polxAple67NNzvpBj7pUZyifunIG8eHJ48130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP557225.RASFiyeJpR0polxAple67NNzvpBj7pUZyifunIG8eHJ48130_provenance.
- NP557225.RASFiyeJpR0polxAple67NNzvpBj7pUZyifunIG8eHJ48130_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." NP557225.RASFiyeJpR0polxAple67NNzvpBj7pUZyifunIG8eHJ48130_provenance.
- NP557225.RASFiyeJpR0polxAple67NNzvpBj7pUZyifunIG8eHJ48130_assertion evidence source_evidence_literature NP557225.RASFiyeJpR0polxAple67NNzvpBj7pUZyifunIG8eHJ48130_provenance.
- NP557225.RASFiyeJpR0polxAple67NNzvpBj7pUZyifunIG8eHJ48130_assertion SIO_000772 16807713 NP557225.RASFiyeJpR0polxAple67NNzvpBj7pUZyifunIG8eHJ48130_provenance.
- NP557225.RASFiyeJpR0polxAple67NNzvpBj7pUZyifunIG8eHJ48130_assertion wasDerivedFrom befree-2016 NP557225.RASFiyeJpR0polxAple67NNzvpBj7pUZyifunIG8eHJ48130_provenance.
- NP557225.RASFiyeJpR0polxAple67NNzvpBj7pUZyifunIG8eHJ48130_assertion wasGeneratedBy ECO_0000203 NP557225.RASFiyeJpR0polxAple67NNzvpBj7pUZyifunIG8eHJ48130_provenance.
- befree-2016 importedOn "2016-02-19" NP557225.RASFiyeJpR0polxAple67NNzvpBj7pUZyifunIG8eHJ48130_provenance.