Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP714164.RAC9N2dxETjV1gYwQXXgIfd6Pluu2IUuClWmD3IbGcX2c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP714164.RAC9N2dxETjV1gYwQXXgIfd6Pluu2IUuClWmD3IbGcX2c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP714164.RAC9N2dxETjV1gYwQXXgIfd6Pluu2IUuClWmD3IbGcX2c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP714164.RAC9N2dxETjV1gYwQXXgIfd6Pluu2IUuClWmD3IbGcX2c130_provenance.
- NP714164.RAC9N2dxETjV1gYwQXXgIfd6Pluu2IUuClWmD3IbGcX2c130_assertion description "[De novo LGI1 mutations of the same kind have also been found in about 2.5% of non-familial cases with idiopathic partial epilepsy with auditory features (IPEAF).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP714164.RAC9N2dxETjV1gYwQXXgIfd6Pluu2IUuClWmD3IbGcX2c130_provenance.
- NP714164.RAC9N2dxETjV1gYwQXXgIfd6Pluu2IUuClWmD3IbGcX2c130_assertion evidence source_evidence_literature NP714164.RAC9N2dxETjV1gYwQXXgIfd6Pluu2IUuClWmD3IbGcX2c130_provenance.
- NP714164.RAC9N2dxETjV1gYwQXXgIfd6Pluu2IUuClWmD3IbGcX2c130_assertion SIO_000772 18355961 NP714164.RAC9N2dxETjV1gYwQXXgIfd6Pluu2IUuClWmD3IbGcX2c130_provenance.
- NP714164.RAC9N2dxETjV1gYwQXXgIfd6Pluu2IUuClWmD3IbGcX2c130_assertion wasDerivedFrom befree-20140225 NP714164.RAC9N2dxETjV1gYwQXXgIfd6Pluu2IUuClWmD3IbGcX2c130_provenance.
- NP714164.RAC9N2dxETjV1gYwQXXgIfd6Pluu2IUuClWmD3IbGcX2c130_assertion wasGeneratedBy ECO_0000203 NP714164.RAC9N2dxETjV1gYwQXXgIfd6Pluu2IUuClWmD3IbGcX2c130_provenance.
- befree-20140225 importedOn "2014-02-25" NP714164.RAC9N2dxETjV1gYwQXXgIfd6Pluu2IUuClWmD3IbGcX2c130_provenance.