Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP632024.RAj60mibPt0lVXtS44mcJH45Ejvu987fhvlO0s8eY3r3M130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP632024.RAj60mibPt0lVXtS44mcJH45Ejvu987fhvlO0s8eY3r3M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP632024.RAj60mibPt0lVXtS44mcJH45Ejvu987fhvlO0s8eY3r3M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP632024.RAj60mibPt0lVXtS44mcJH45Ejvu987fhvlO0s8eY3r3M130_provenance.
- NP632024.RAj60mibPt0lVXtS44mcJH45Ejvu987fhvlO0s8eY3r3M130_assertion description "[Here we describe identification of the causative gene in autosomal-dominant partial epilepsy with auditory features (ADPEAF, MIM 600512), a rare form of idiopathic lateral temporal lobe epilepsy characterized by partial seizures with auditory disturbances.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP632024.RAj60mibPt0lVXtS44mcJH45Ejvu987fhvlO0s8eY3r3M130_provenance.
- NP632024.RAj60mibPt0lVXtS44mcJH45Ejvu987fhvlO0s8eY3r3M130_assertion evidence source_evidence_literature NP632024.RAj60mibPt0lVXtS44mcJH45Ejvu987fhvlO0s8eY3r3M130_provenance.
- NP632024.RAj60mibPt0lVXtS44mcJH45Ejvu987fhvlO0s8eY3r3M130_assertion SIO_000772 11810107 NP632024.RAj60mibPt0lVXtS44mcJH45Ejvu987fhvlO0s8eY3r3M130_provenance.
- NP632024.RAj60mibPt0lVXtS44mcJH45Ejvu987fhvlO0s8eY3r3M130_assertion wasDerivedFrom befree-20140225 NP632024.RAj60mibPt0lVXtS44mcJH45Ejvu987fhvlO0s8eY3r3M130_provenance.
- NP632024.RAj60mibPt0lVXtS44mcJH45Ejvu987fhvlO0s8eY3r3M130_assertion wasGeneratedBy ECO_0000203 NP632024.RAj60mibPt0lVXtS44mcJH45Ejvu987fhvlO0s8eY3r3M130_provenance.
- befree-20140225 importedOn "2014-02-25" NP632024.RAj60mibPt0lVXtS44mcJH45Ejvu987fhvlO0s8eY3r3M130_provenance.