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- NP311447.RA1g59theGPYO3-efWGIekbMc6GJflLcuyJwuxFyZSW9I130_assertion type Assertion NP311447.RA1g59theGPYO3-efWGIekbMc6GJflLcuyJwuxFyZSW9I130_head.
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- NP311447.RA1g59theGPYO3-efWGIekbMc6GJflLcuyJwuxFyZSW9I130_assertion wasDerivedFrom befree-2016 NP311447.RA1g59theGPYO3-efWGIekbMc6GJflLcuyJwuxFyZSW9I130_provenance.
- NP311447.RA1g59theGPYO3-efWGIekbMc6GJflLcuyJwuxFyZSW9I130_assertion SIO_000772 11257260 NP311447.RA1g59theGPYO3-efWGIekbMc6GJflLcuyJwuxFyZSW9I130_provenance.
- NP311447.RA1g59theGPYO3-efWGIekbMc6GJflLcuyJwuxFyZSW9I130_assertion evidence source_evidence_literature NP311447.RA1g59theGPYO3-efWGIekbMc6GJflLcuyJwuxFyZSW9I130_provenance.
- NP311447.RA1g59theGPYO3-efWGIekbMc6GJflLcuyJwuxFyZSW9I130_assertion description "[A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311447.RA1g59theGPYO3-efWGIekbMc6GJflLcuyJwuxFyZSW9I130_provenance.