Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1231789.RAmW9FqVgzIy001GeunHLO-vSdgXWBCvZgc353ZQxUoqo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1231789.RAmW9FqVgzIy001GeunHLO-vSdgXWBCvZgc353ZQxUoqo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1231789.RAmW9FqVgzIy001GeunHLO-vSdgXWBCvZgc353ZQxUoqo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1231789.RAmW9FqVgzIy001GeunHLO-vSdgXWBCvZgc353ZQxUoqo130_provenance.
- NP1231789.RAmW9FqVgzIy001GeunHLO-vSdgXWBCvZgc353ZQxUoqo130_assertion description "[Some of the rare genetic epilepsies enable treatment stratification through testing for the causal mutation, for example SCN1A mutations in patients with Dravet's syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1231789.RAmW9FqVgzIy001GeunHLO-vSdgXWBCvZgc353ZQxUoqo130_provenance.
- NP1231789.RAmW9FqVgzIy001GeunHLO-vSdgXWBCvZgc353ZQxUoqo130_assertion evidence source_evidence_literature NP1231789.RAmW9FqVgzIy001GeunHLO-vSdgXWBCvZgc353ZQxUoqo130_provenance.
- NP1231789.RAmW9FqVgzIy001GeunHLO-vSdgXWBCvZgc353ZQxUoqo130_assertion SIO_000772 25338670 NP1231789.RAmW9FqVgzIy001GeunHLO-vSdgXWBCvZgc353ZQxUoqo130_provenance.
- NP1231789.RAmW9FqVgzIy001GeunHLO-vSdgXWBCvZgc353ZQxUoqo130_assertion wasDerivedFrom befree-2016 NP1231789.RAmW9FqVgzIy001GeunHLO-vSdgXWBCvZgc353ZQxUoqo130_provenance.
- NP1231789.RAmW9FqVgzIy001GeunHLO-vSdgXWBCvZgc353ZQxUoqo130_assertion wasGeneratedBy ECO_0000203 NP1231789.RAmW9FqVgzIy001GeunHLO-vSdgXWBCvZgc353ZQxUoqo130_provenance.
- befree-2016 importedOn "2016-02-19" NP1231789.RAmW9FqVgzIy001GeunHLO-vSdgXWBCvZgc353ZQxUoqo130_provenance.