Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP5670.RAR4THIyOIBPpbe8qcHkSP5FbZyituM8HTZBpkQywTdEg130_assertion> ?p ?o ?g. }
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- NP5670.RAR4THIyOIBPpbe8qcHkSP5FbZyituM8HTZBpkQywTdEg130_assertion type Assertion NP5670.RAR4THIyOIBPpbe8qcHkSP5FbZyituM8HTZBpkQywTdEg130_head.
- NP5670.RAR4THIyOIBPpbe8qcHkSP5FbZyituM8HTZBpkQywTdEg130_assertion wasGeneratedBy ECO_0000218 NP5670.RAR4THIyOIBPpbe8qcHkSP5FbZyituM8HTZBpkQywTdEg130_provenance.
- NP5670.RAR4THIyOIBPpbe8qcHkSP5FbZyituM8HTZBpkQywTdEg130_assertion wasDerivedFrom uniprot-2016 NP5670.RAR4THIyOIBPpbe8qcHkSP5FbZyituM8HTZBpkQywTdEg130_provenance.
- NP5670.RAR4THIyOIBPpbe8qcHkSP5FbZyituM8HTZBpkQywTdEg130_assertion SIO_000772 19191227 NP5670.RAR4THIyOIBPpbe8qcHkSP5FbZyituM8HTZBpkQywTdEg130_provenance.
- NP5670.RAR4THIyOIBPpbe8qcHkSP5FbZyituM8HTZBpkQywTdEg130_assertion evidence source_evidence_curated NP5670.RAR4THIyOIBPpbe8qcHkSP5FbZyituM8HTZBpkQywTdEg130_provenance.
- NP5670.RAR4THIyOIBPpbe8qcHkSP5FbZyituM8HTZBpkQywTdEg130_assertion description "[In addition, de novo LGI1 mutations are found in about 2% of sporadic cases with idiopathic partial epilepsy with auditory features, who are clinically similar to the majority of patients with ADLTE/ADPEAF but have no family history.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5670.RAR4THIyOIBPpbe8qcHkSP5FbZyituM8HTZBpkQywTdEg130_provenance.