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- NP682489.RAPfOYjJn3HAHHp-AeYjcRcCkW6hajj5l9x48wjhsVPxI130_assertion type Assertion NP682489.RAPfOYjJn3HAHHp-AeYjcRcCkW6hajj5l9x48wjhsVPxI130_head.
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- NP682489.RAPfOYjJn3HAHHp-AeYjcRcCkW6hajj5l9x48wjhsVPxI130_assertion wasDerivedFrom befree-20150227 NP682489.RAPfOYjJn3HAHHp-AeYjcRcCkW6hajj5l9x48wjhsVPxI130_provenance.
- NP682489.RAPfOYjJn3HAHHp-AeYjcRcCkW6hajj5l9x48wjhsVPxI130_assertion SIO_000772 21855646 NP682489.RAPfOYjJn3HAHHp-AeYjcRcCkW6hajj5l9x48wjhsVPxI130_provenance.
- NP682489.RAPfOYjJn3HAHHp-AeYjcRcCkW6hajj5l9x48wjhsVPxI130_assertion evidence source_evidence_literature NP682489.RAPfOYjJn3HAHHp-AeYjcRcCkW6hajj5l9x48wjhsVPxI130_provenance.
- NP682489.RAPfOYjJn3HAHHp-AeYjcRcCkW6hajj5l9x48wjhsVPxI130_assertion description "[Genetic studies have identified mutations in the CACNA1, ATP1A2 and SCN1A genes in the rare familial hemiplegic migraine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682489.RAPfOYjJn3HAHHp-AeYjcRcCkW6hajj5l9x48wjhsVPxI130_provenance.