Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP523313.RAnlhau1oFwi0OqUiQyL8WJ8tTJe03TmUG_bbi8wZDOWg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP523313.RAnlhau1oFwi0OqUiQyL8WJ8tTJe03TmUG_bbi8wZDOWg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP523313.RAnlhau1oFwi0OqUiQyL8WJ8tTJe03TmUG_bbi8wZDOWg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP523313.RAnlhau1oFwi0OqUiQyL8WJ8tTJe03TmUG_bbi8wZDOWg130_provenance.
- NP523313.RAnlhau1oFwi0OqUiQyL8WJ8tTJe03TmUG_bbi8wZDOWg130_assertion description "[Array comparative genomic hybridization (CGH) demonstrated a 1.5-Mb terminal deletion of the long arm of chromosome 20, which included deletion of the KCNQ2 and CHRNA4 genes, both of which have been associated with specific epilepsy syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523313.RAnlhau1oFwi0OqUiQyL8WJ8tTJe03TmUG_bbi8wZDOWg130_provenance.
- NP523313.RAnlhau1oFwi0OqUiQyL8WJ8tTJe03TmUG_bbi8wZDOWg130_assertion evidence source_evidence_literature NP523313.RAnlhau1oFwi0OqUiQyL8WJ8tTJe03TmUG_bbi8wZDOWg130_provenance.
- NP523313.RAnlhau1oFwi0OqUiQyL8WJ8tTJe03TmUG_bbi8wZDOWg130_assertion SIO_000772 23166088 NP523313.RAnlhau1oFwi0OqUiQyL8WJ8tTJe03TmUG_bbi8wZDOWg130_provenance.
- NP523313.RAnlhau1oFwi0OqUiQyL8WJ8tTJe03TmUG_bbi8wZDOWg130_assertion wasDerivedFrom befree-20150227 NP523313.RAnlhau1oFwi0OqUiQyL8WJ8tTJe03TmUG_bbi8wZDOWg130_provenance.
- NP523313.RAnlhau1oFwi0OqUiQyL8WJ8tTJe03TmUG_bbi8wZDOWg130_assertion wasGeneratedBy ECO_0000203 NP523313.RAnlhau1oFwi0OqUiQyL8WJ8tTJe03TmUG_bbi8wZDOWg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP523313.RAnlhau1oFwi0OqUiQyL8WJ8tTJe03TmUG_bbi8wZDOWg130_provenance.