Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP619468.RAFh5Wo0D0D7nc5RT7FofOoxx3B2_JQuEYzfDStYNEYOc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP619468.RAFh5Wo0D0D7nc5RT7FofOoxx3B2_JQuEYzfDStYNEYOc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP619468.RAFh5Wo0D0D7nc5RT7FofOoxx3B2_JQuEYzfDStYNEYOc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP619468.RAFh5Wo0D0D7nc5RT7FofOoxx3B2_JQuEYzfDStYNEYOc130_provenance.
- NP619468.RAFh5Wo0D0D7nc5RT7FofOoxx3B2_JQuEYzfDStYNEYOc130_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." NP619468.RAFh5Wo0D0D7nc5RT7FofOoxx3B2_JQuEYzfDStYNEYOc130_provenance.
- NP619468.RAFh5Wo0D0D7nc5RT7FofOoxx3B2_JQuEYzfDStYNEYOc130_assertion evidence source_evidence_literature NP619468.RAFh5Wo0D0D7nc5RT7FofOoxx3B2_JQuEYzfDStYNEYOc130_provenance.
- NP619468.RAFh5Wo0D0D7nc5RT7FofOoxx3B2_JQuEYzfDStYNEYOc130_assertion SIO_000772 17981785 NP619468.RAFh5Wo0D0D7nc5RT7FofOoxx3B2_JQuEYzfDStYNEYOc130_provenance.
- NP619468.RAFh5Wo0D0D7nc5RT7FofOoxx3B2_JQuEYzfDStYNEYOc130_assertion wasDerivedFrom befree-20140225 NP619468.RAFh5Wo0D0D7nc5RT7FofOoxx3B2_JQuEYzfDStYNEYOc130_provenance.
- NP619468.RAFh5Wo0D0D7nc5RT7FofOoxx3B2_JQuEYzfDStYNEYOc130_assertion wasGeneratedBy ECO_0000203 NP619468.RAFh5Wo0D0D7nc5RT7FofOoxx3B2_JQuEYzfDStYNEYOc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP619468.RAFh5Wo0D0D7nc5RT7FofOoxx3B2_JQuEYzfDStYNEYOc130_provenance.