Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP927771.RAthXHuB3gVMS-X4laHQn6USupQb1HfhnxvQq7UuC9JlU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP927771.RAthXHuB3gVMS-X4laHQn6USupQb1HfhnxvQq7UuC9JlU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP927771.RAthXHuB3gVMS-X4laHQn6USupQb1HfhnxvQq7UuC9JlU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP927771.RAthXHuB3gVMS-X4laHQn6USupQb1HfhnxvQq7UuC9JlU130_provenance.
- NP927771.RAthXHuB3gVMS-X4laHQn6USupQb1HfhnxvQq7UuC9JlU130_assertion description "[Mutation of LGI1 gene has been identified in familial lateral temporal lobe epilepsy while mutations of genes which encode sodium channels and GABAA receptors have been reported in generalized epilepsy with febrile seizure plus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP927771.RAthXHuB3gVMS-X4laHQn6USupQb1HfhnxvQq7UuC9JlU130_provenance.
- NP927771.RAthXHuB3gVMS-X4laHQn6USupQb1HfhnxvQq7UuC9JlU130_assertion evidence source_evidence_literature NP927771.RAthXHuB3gVMS-X4laHQn6USupQb1HfhnxvQq7UuC9JlU130_provenance.
- NP927771.RAthXHuB3gVMS-X4laHQn6USupQb1HfhnxvQq7UuC9JlU130_assertion SIO_000772 17981785 NP927771.RAthXHuB3gVMS-X4laHQn6USupQb1HfhnxvQq7UuC9JlU130_provenance.
- NP927771.RAthXHuB3gVMS-X4laHQn6USupQb1HfhnxvQq7UuC9JlU130_assertion wasDerivedFrom befree-20140225 NP927771.RAthXHuB3gVMS-X4laHQn6USupQb1HfhnxvQq7UuC9JlU130_provenance.
- NP927771.RAthXHuB3gVMS-X4laHQn6USupQb1HfhnxvQq7UuC9JlU130_assertion wasGeneratedBy ECO_0000203 NP927771.RAthXHuB3gVMS-X4laHQn6USupQb1HfhnxvQq7UuC9JlU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP927771.RAthXHuB3gVMS-X4laHQn6USupQb1HfhnxvQq7UuC9JlU130_provenance.