Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP185625.RAs3lxhUrQh5xX7vH1HPp3SRi3PkVfnlWzMD2llN4UarY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP185625.RAs3lxhUrQh5xX7vH1HPp3SRi3PkVfnlWzMD2llN4UarY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP185625.RAs3lxhUrQh5xX7vH1HPp3SRi3PkVfnlWzMD2llN4UarY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP185625.RAs3lxhUrQh5xX7vH1HPp3SRi3PkVfnlWzMD2llN4UarY130_provenance.
- NP185625.RAs3lxhUrQh5xX7vH1HPp3SRi3PkVfnlWzMD2llN4UarY130_assertion description "[This paper summarizes recent findings concerning sodium (SCN1A) and potassium channel (KCNQ2 and KCNQ3) dysfunctions in the pathogenesis of rare and common idiopathic epilepsies (IE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185625.RAs3lxhUrQh5xX7vH1HPp3SRi3PkVfnlWzMD2llN4UarY130_provenance.
- NP185625.RAs3lxhUrQh5xX7vH1HPp3SRi3PkVfnlWzMD2llN4UarY130_assertion evidence source_evidence_literature NP185625.RAs3lxhUrQh5xX7vH1HPp3SRi3PkVfnlWzMD2llN4UarY130_provenance.
- NP185625.RAs3lxhUrQh5xX7vH1HPp3SRi3PkVfnlWzMD2llN4UarY130_assertion SIO_000772 19464834 NP185625.RAs3lxhUrQh5xX7vH1HPp3SRi3PkVfnlWzMD2llN4UarY130_provenance.
- NP185625.RAs3lxhUrQh5xX7vH1HPp3SRi3PkVfnlWzMD2llN4UarY130_assertion wasDerivedFrom befree-20140225 NP185625.RAs3lxhUrQh5xX7vH1HPp3SRi3PkVfnlWzMD2llN4UarY130_provenance.
- NP185625.RAs3lxhUrQh5xX7vH1HPp3SRi3PkVfnlWzMD2llN4UarY130_assertion wasGeneratedBy ECO_0000203 NP185625.RAs3lxhUrQh5xX7vH1HPp3SRi3PkVfnlWzMD2llN4UarY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP185625.RAs3lxhUrQh5xX7vH1HPp3SRi3PkVfnlWzMD2llN4UarY130_provenance.