Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP783671.RAW8AzJb0AZSVJHzhLy9JRE2NwKjqx-ZbDN9M0MPYVi58130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP783671.RAW8AzJb0AZSVJHzhLy9JRE2NwKjqx-ZbDN9M0MPYVi58130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP783671.RAW8AzJb0AZSVJHzhLy9JRE2NwKjqx-ZbDN9M0MPYVi58130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP783671.RAW8AzJb0AZSVJHzhLy9JRE2NwKjqx-ZbDN9M0MPYVi58130_provenance.
- NP783671.RAW8AzJb0AZSVJHzhLy9JRE2NwKjqx-ZbDN9M0MPYVi58130_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." NP783671.RAW8AzJb0AZSVJHzhLy9JRE2NwKjqx-ZbDN9M0MPYVi58130_provenance.
- NP783671.RAW8AzJb0AZSVJHzhLy9JRE2NwKjqx-ZbDN9M0MPYVi58130_assertion evidence source_evidence_literature NP783671.RAW8AzJb0AZSVJHzhLy9JRE2NwKjqx-ZbDN9M0MPYVi58130_provenance.
- NP783671.RAW8AzJb0AZSVJHzhLy9JRE2NwKjqx-ZbDN9M0MPYVi58130_assertion SIO_000772 16807713 NP783671.RAW8AzJb0AZSVJHzhLy9JRE2NwKjqx-ZbDN9M0MPYVi58130_provenance.
- NP783671.RAW8AzJb0AZSVJHzhLy9JRE2NwKjqx-ZbDN9M0MPYVi58130_assertion wasDerivedFrom befree-20140225 NP783671.RAW8AzJb0AZSVJHzhLy9JRE2NwKjqx-ZbDN9M0MPYVi58130_provenance.
- NP783671.RAW8AzJb0AZSVJHzhLy9JRE2NwKjqx-ZbDN9M0MPYVi58130_assertion wasGeneratedBy ECO_0000203 NP783671.RAW8AzJb0AZSVJHzhLy9JRE2NwKjqx-ZbDN9M0MPYVi58130_provenance.
- befree-20140225 importedOn "2014-02-25" NP783671.RAW8AzJb0AZSVJHzhLy9JRE2NwKjqx-ZbDN9M0MPYVi58130_provenance.