Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP714164.RAC9N2dxETjV1gYwQXXgIfd6Pluu2IUuClWmD3IbGcX2c130_assertion> ?p ?o ?g. }
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- NP714164.RAC9N2dxETjV1gYwQXXgIfd6Pluu2IUuClWmD3IbGcX2c130_assertion type Assertion NP714164.RAC9N2dxETjV1gYwQXXgIfd6Pluu2IUuClWmD3IbGcX2c130_head.
- 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.