Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP436368.RA_uTLnxiOsjaG3loETVXewavRl6JJJk6W0IZMvJVcJwU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP436368.RA_uTLnxiOsjaG3loETVXewavRl6JJJk6W0IZMvJVcJwU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP436368.RA_uTLnxiOsjaG3loETVXewavRl6JJJk6W0IZMvJVcJwU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP436368.RA_uTLnxiOsjaG3loETVXewavRl6JJJk6W0IZMvJVcJwU130_provenance.
- NP436368.RA_uTLnxiOsjaG3loETVXewavRl6JJJk6W0IZMvJVcJwU130_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." NP436368.RA_uTLnxiOsjaG3loETVXewavRl6JJJk6W0IZMvJVcJwU130_provenance.
- NP436368.RA_uTLnxiOsjaG3loETVXewavRl6JJJk6W0IZMvJVcJwU130_assertion evidence source_evidence_literature NP436368.RA_uTLnxiOsjaG3loETVXewavRl6JJJk6W0IZMvJVcJwU130_provenance.
- NP436368.RA_uTLnxiOsjaG3loETVXewavRl6JJJk6W0IZMvJVcJwU130_assertion SIO_000772 19576955 NP436368.RA_uTLnxiOsjaG3loETVXewavRl6JJJk6W0IZMvJVcJwU130_provenance.
- NP436368.RA_uTLnxiOsjaG3loETVXewavRl6JJJk6W0IZMvJVcJwU130_assertion wasDerivedFrom befree-20140225 NP436368.RA_uTLnxiOsjaG3loETVXewavRl6JJJk6W0IZMvJVcJwU130_provenance.
- NP436368.RA_uTLnxiOsjaG3loETVXewavRl6JJJk6W0IZMvJVcJwU130_assertion wasGeneratedBy ECO_0000203 NP436368.RA_uTLnxiOsjaG3loETVXewavRl6JJJk6W0IZMvJVcJwU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP436368.RA_uTLnxiOsjaG3loETVXewavRl6JJJk6W0IZMvJVcJwU130_provenance.