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- NP521298.RAimeYOnTsmdjYLKY_zfdlQXP1CVrHSnrNQB0_3yeN_o8130_assertion type Assertion NP521298.RAimeYOnTsmdjYLKY_zfdlQXP1CVrHSnrNQB0_3yeN_o8130_head.
- NP521298.RAimeYOnTsmdjYLKY_zfdlQXP1CVrHSnrNQB0_3yeN_o8130_assertion wasGeneratedBy ECO_0000203 NP521298.RAimeYOnTsmdjYLKY_zfdlQXP1CVrHSnrNQB0_3yeN_o8130_provenance.
- NP521298.RAimeYOnTsmdjYLKY_zfdlQXP1CVrHSnrNQB0_3yeN_o8130_assertion wasDerivedFrom befree-20150227 NP521298.RAimeYOnTsmdjYLKY_zfdlQXP1CVrHSnrNQB0_3yeN_o8130_provenance.
- NP521298.RAimeYOnTsmdjYLKY_zfdlQXP1CVrHSnrNQB0_3yeN_o8130_assertion SIO_000772 17136396 NP521298.RAimeYOnTsmdjYLKY_zfdlQXP1CVrHSnrNQB0_3yeN_o8130_provenance.
- NP521298.RAimeYOnTsmdjYLKY_zfdlQXP1CVrHSnrNQB0_3yeN_o8130_assertion evidence source_evidence_literature NP521298.RAimeYOnTsmdjYLKY_zfdlQXP1CVrHSnrNQB0_3yeN_o8130_provenance.
- NP521298.RAimeYOnTsmdjYLKY_zfdlQXP1CVrHSnrNQB0_3yeN_o8130_assertion description "[Functional analysis of a novel potassium channel (KCNA1) mutation in hereditary myokymia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP521298.RAimeYOnTsmdjYLKY_zfdlQXP1CVrHSnrNQB0_3yeN_o8130_provenance.