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- NP718520.RA34JVB8UQa572dW-QN1h87hOiL2wKJCaJk0cMJbrk2Nw130_assertion type Assertion NP718520.RA34JVB8UQa572dW-QN1h87hOiL2wKJCaJk0cMJbrk2Nw130_head.
- NP718520.RA34JVB8UQa572dW-QN1h87hOiL2wKJCaJk0cMJbrk2Nw130_assertion wasGeneratedBy ECO_0000203 NP718520.RA34JVB8UQa572dW-QN1h87hOiL2wKJCaJk0cMJbrk2Nw130_provenance.
- NP718520.RA34JVB8UQa572dW-QN1h87hOiL2wKJCaJk0cMJbrk2Nw130_assertion wasDerivedFrom befree-2016 NP718520.RA34JVB8UQa572dW-QN1h87hOiL2wKJCaJk0cMJbrk2Nw130_provenance.
- NP718520.RA34JVB8UQa572dW-QN1h87hOiL2wKJCaJk0cMJbrk2Nw130_assertion SIO_000772 19191227 NP718520.RA34JVB8UQa572dW-QN1h87hOiL2wKJCaJk0cMJbrk2Nw130_provenance.
- NP718520.RA34JVB8UQa572dW-QN1h87hOiL2wKJCaJk0cMJbrk2Nw130_assertion evidence source_evidence_literature NP718520.RA34JVB8UQa572dW-QN1h87hOiL2wKJCaJk0cMJbrk2Nw130_provenance.
- NP718520.RA34JVB8UQa572dW-QN1h87hOiL2wKJCaJk0cMJbrk2Nw130_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." NP718520.RA34JVB8UQa572dW-QN1h87hOiL2wKJCaJk0cMJbrk2Nw130_provenance.