Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP990286.RAv3wm74ajiqz2vmDZsuLNHeTNklKsq0nZnWsoElVGqD0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP990286.RAv3wm74ajiqz2vmDZsuLNHeTNklKsq0nZnWsoElVGqD0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP990286.RAv3wm74ajiqz2vmDZsuLNHeTNklKsq0nZnWsoElVGqD0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP990286.RAv3wm74ajiqz2vmDZsuLNHeTNklKsq0nZnWsoElVGqD0130_provenance.
- NP990286.RAv3wm74ajiqz2vmDZsuLNHeTNklKsq0nZnWsoElVGqD0130_assertion description "[To review three inherited retinal disorders associated with diagnostic or pathognomonic electroretinogram (ERG) abnormalities: cone dystrophy with supernormal rod ERG (KCNV2), enhanced S-cone syndrome (NR2E3), and bradyopsia (RGS9/R9AP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP990286.RAv3wm74ajiqz2vmDZsuLNHeTNklKsq0nZnWsoElVGqD0130_provenance.
- NP990286.RAv3wm74ajiqz2vmDZsuLNHeTNklKsq0nZnWsoElVGqD0130_assertion evidence source_evidence_literature NP990286.RAv3wm74ajiqz2vmDZsuLNHeTNklKsq0nZnWsoElVGqD0130_provenance.
- NP990286.RAv3wm74ajiqz2vmDZsuLNHeTNklKsq0nZnWsoElVGqD0130_assertion SIO_000772 23263253 NP990286.RAv3wm74ajiqz2vmDZsuLNHeTNklKsq0nZnWsoElVGqD0130_provenance.
- NP990286.RAv3wm74ajiqz2vmDZsuLNHeTNklKsq0nZnWsoElVGqD0130_assertion wasDerivedFrom befree-20150227 NP990286.RAv3wm74ajiqz2vmDZsuLNHeTNklKsq0nZnWsoElVGqD0130_provenance.
- NP990286.RAv3wm74ajiqz2vmDZsuLNHeTNklKsq0nZnWsoElVGqD0130_assertion wasGeneratedBy ECO_0000203 NP990286.RAv3wm74ajiqz2vmDZsuLNHeTNklKsq0nZnWsoElVGqD0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP990286.RAv3wm74ajiqz2vmDZsuLNHeTNklKsq0nZnWsoElVGqD0130_provenance.