Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP651448.RA8tAlYykDQRyNw530b139xA6qvQEeJ2kpYfZ0Gd0-NfY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP651448.RA8tAlYykDQRyNw530b139xA6qvQEeJ2kpYfZ0Gd0-NfY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP651448.RA8tAlYykDQRyNw530b139xA6qvQEeJ2kpYfZ0Gd0-NfY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP651448.RA8tAlYykDQRyNw530b139xA6qvQEeJ2kpYfZ0Gd0-NfY130_provenance.
- NP651448.RA8tAlYykDQRyNw530b139xA6qvQEeJ2kpYfZ0Gd0-NfY130_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." NP651448.RA8tAlYykDQRyNw530b139xA6qvQEeJ2kpYfZ0Gd0-NfY130_provenance.
- NP651448.RA8tAlYykDQRyNw530b139xA6qvQEeJ2kpYfZ0Gd0-NfY130_assertion evidence source_evidence_literature NP651448.RA8tAlYykDQRyNw530b139xA6qvQEeJ2kpYfZ0Gd0-NfY130_provenance.
- NP651448.RA8tAlYykDQRyNw530b139xA6qvQEeJ2kpYfZ0Gd0-NfY130_assertion SIO_000772 19576955 NP651448.RA8tAlYykDQRyNw530b139xA6qvQEeJ2kpYfZ0Gd0-NfY130_provenance.
- NP651448.RA8tAlYykDQRyNw530b139xA6qvQEeJ2kpYfZ0Gd0-NfY130_assertion wasDerivedFrom befree-20140225 NP651448.RA8tAlYykDQRyNw530b139xA6qvQEeJ2kpYfZ0Gd0-NfY130_provenance.
- NP651448.RA8tAlYykDQRyNw530b139xA6qvQEeJ2kpYfZ0Gd0-NfY130_assertion wasGeneratedBy ECO_0000203 NP651448.RA8tAlYykDQRyNw530b139xA6qvQEeJ2kpYfZ0Gd0-NfY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP651448.RA8tAlYykDQRyNw530b139xA6qvQEeJ2kpYfZ0Gd0-NfY130_provenance.