Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP587556.RAz6UlYAID9HUCLV0DXsvB-KuKzjCX4rrEyE6P_tQo8TQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP587556.RAz6UlYAID9HUCLV0DXsvB-KuKzjCX4rrEyE6P_tQo8TQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP587556.RAz6UlYAID9HUCLV0DXsvB-KuKzjCX4rrEyE6P_tQo8TQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP587556.RAz6UlYAID9HUCLV0DXsvB-KuKzjCX4rrEyE6P_tQo8TQ130_provenance.
- NP587556.RAz6UlYAID9HUCLV0DXsvB-KuKzjCX4rrEyE6P_tQo8TQ130_assertion description "[The DQB1*0602 association was highest in cases with hypocretin deficiency (100% vs 13% in controls), most of which had narcolepsy-cataplexy (81%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP587556.RAz6UlYAID9HUCLV0DXsvB-KuKzjCX4rrEyE6P_tQo8TQ130_provenance.
- NP587556.RAz6UlYAID9HUCLV0DXsvB-KuKzjCX4rrEyE6P_tQo8TQ130_assertion evidence source_evidence_literature NP587556.RAz6UlYAID9HUCLV0DXsvB-KuKzjCX4rrEyE6P_tQo8TQ130_provenance.
- NP587556.RAz6UlYAID9HUCLV0DXsvB-KuKzjCX4rrEyE6P_tQo8TQ130_assertion SIO_000772 17207713 NP587556.RAz6UlYAID9HUCLV0DXsvB-KuKzjCX4rrEyE6P_tQo8TQ130_provenance.
- NP587556.RAz6UlYAID9HUCLV0DXsvB-KuKzjCX4rrEyE6P_tQo8TQ130_assertion wasDerivedFrom befree-2016 NP587556.RAz6UlYAID9HUCLV0DXsvB-KuKzjCX4rrEyE6P_tQo8TQ130_provenance.
- NP587556.RAz6UlYAID9HUCLV0DXsvB-KuKzjCX4rrEyE6P_tQo8TQ130_assertion wasGeneratedBy ECO_0000203 NP587556.RAz6UlYAID9HUCLV0DXsvB-KuKzjCX4rrEyE6P_tQo8TQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP587556.RAz6UlYAID9HUCLV0DXsvB-KuKzjCX4rrEyE6P_tQo8TQ130_provenance.