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- NP523319.RAXXg6p6buJPrwSeiHbes5Ip3W0o_lZglDfKzEguDkjWg130_assertion type Assertion NP523319.RAXXg6p6buJPrwSeiHbes5Ip3W0o_lZglDfKzEguDkjWg130_head.
- NP523319.RAXXg6p6buJPrwSeiHbes5Ip3W0o_lZglDfKzEguDkjWg130_assertion description "[Mutations in the potassium channel subunit KCNQ2 lead to benign familial neonatal convulsions, a dominantly inherited form of generalized epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523319.RAXXg6p6buJPrwSeiHbes5Ip3W0o_lZglDfKzEguDkjWg130_provenance.
- NP523319.RAXXg6p6buJPrwSeiHbes5Ip3W0o_lZglDfKzEguDkjWg130_assertion evidence source_evidence_literature NP523319.RAXXg6p6buJPrwSeiHbes5Ip3W0o_lZglDfKzEguDkjWg130_provenance.
- NP523319.RAXXg6p6buJPrwSeiHbes5Ip3W0o_lZglDfKzEguDkjWg130_assertion SIO_000772 11739564 NP523319.RAXXg6p6buJPrwSeiHbes5Ip3W0o_lZglDfKzEguDkjWg130_provenance.
- NP523319.RAXXg6p6buJPrwSeiHbes5Ip3W0o_lZglDfKzEguDkjWg130_assertion wasDerivedFrom befree-20150227 NP523319.RAXXg6p6buJPrwSeiHbes5Ip3W0o_lZglDfKzEguDkjWg130_provenance.
- NP523319.RAXXg6p6buJPrwSeiHbes5Ip3W0o_lZglDfKzEguDkjWg130_assertion wasGeneratedBy ECO_0000203 NP523319.RAXXg6p6buJPrwSeiHbes5Ip3W0o_lZglDfKzEguDkjWg130_provenance.