Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP190178.RAbEHZu0005K_omH5n4PoYiNKTSFn4XWSKqGG4gASkiGQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP190178.RAbEHZu0005K_omH5n4PoYiNKTSFn4XWSKqGG4gASkiGQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP190178.RAbEHZu0005K_omH5n4PoYiNKTSFn4XWSKqGG4gASkiGQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP190178.RAbEHZu0005K_omH5n4PoYiNKTSFn4XWSKqGG4gASkiGQ130_provenance.
- NP190178.RAbEHZu0005K_omH5n4PoYiNKTSFn4XWSKqGG4gASkiGQ130_assertion description "[Mutations in the EFHC1 gene may underlie different types of epilepsy syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP190178.RAbEHZu0005K_omH5n4PoYiNKTSFn4XWSKqGG4gASkiGQ130_provenance.
- NP190178.RAbEHZu0005K_omH5n4PoYiNKTSFn4XWSKqGG4gASkiGQ130_assertion evidence source_evidence_literature NP190178.RAbEHZu0005K_omH5n4PoYiNKTSFn4XWSKqGG4gASkiGQ130_provenance.
- NP190178.RAbEHZu0005K_omH5n4PoYiNKTSFn4XWSKqGG4gASkiGQ130_assertion SIO_000772 17159113 NP190178.RAbEHZu0005K_omH5n4PoYiNKTSFn4XWSKqGG4gASkiGQ130_provenance.
- NP190178.RAbEHZu0005K_omH5n4PoYiNKTSFn4XWSKqGG4gASkiGQ130_assertion wasDerivedFrom lhgdn-20090331 NP190178.RAbEHZu0005K_omH5n4PoYiNKTSFn4XWSKqGG4gASkiGQ130_provenance.
- NP190178.RAbEHZu0005K_omH5n4PoYiNKTSFn4XWSKqGG4gASkiGQ130_assertion wasGeneratedBy ECO_0000203 NP190178.RAbEHZu0005K_omH5n4PoYiNKTSFn4XWSKqGG4gASkiGQ130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP190178.RAbEHZu0005K_omH5n4PoYiNKTSFn4XWSKqGG4gASkiGQ130_provenance.