Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP682715.RAtIqQ-p3thoyyu3TrSNtfE-9ROgbgs-5X-xv9glsVI5c130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP682715.RAtIqQ-p3thoyyu3TrSNtfE-9ROgbgs-5X-xv9glsVI5c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP682715.RAtIqQ-p3thoyyu3TrSNtfE-9ROgbgs-5X-xv9glsVI5c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP682715.RAtIqQ-p3thoyyu3TrSNtfE-9ROgbgs-5X-xv9glsVI5c130_provenance.
- NP682715.RAtIqQ-p3thoyyu3TrSNtfE-9ROgbgs-5X-xv9glsVI5c130_assertion description "[Lack of evidence for association between D2S124 and D2S111 polymorphisms of the SCN2A gene and idiopathic generalized epilepsy with generalized tonic clonic seizures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682715.RAtIqQ-p3thoyyu3TrSNtfE-9ROgbgs-5X-xv9glsVI5c130_provenance.
- NP682715.RAtIqQ-p3thoyyu3TrSNtfE-9ROgbgs-5X-xv9glsVI5c130_assertion evidence source_evidence_literature NP682715.RAtIqQ-p3thoyyu3TrSNtfE-9ROgbgs-5X-xv9glsVI5c130_provenance.
- NP682715.RAtIqQ-p3thoyyu3TrSNtfE-9ROgbgs-5X-xv9glsVI5c130_assertion SIO_000772 17715289 NP682715.RAtIqQ-p3thoyyu3TrSNtfE-9ROgbgs-5X-xv9glsVI5c130_provenance.
- NP682715.RAtIqQ-p3thoyyu3TrSNtfE-9ROgbgs-5X-xv9glsVI5c130_assertion wasDerivedFrom befree-20150227 NP682715.RAtIqQ-p3thoyyu3TrSNtfE-9ROgbgs-5X-xv9glsVI5c130_provenance.
- NP682715.RAtIqQ-p3thoyyu3TrSNtfE-9ROgbgs-5X-xv9glsVI5c130_assertion wasGeneratedBy ECO_0000203 NP682715.RAtIqQ-p3thoyyu3TrSNtfE-9ROgbgs-5X-xv9glsVI5c130_provenance.
- befree-20150227 importedOn "2015-02-27" NP682715.RAtIqQ-p3thoyyu3TrSNtfE-9ROgbgs-5X-xv9glsVI5c130_provenance.