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Q22008704-3D1FA4E5-BBDC-4CA7-B237-43DCDCD0DC56
Q22008704-3D1FA4E5-BBDC-4CA7-B237-43DCDCD0DC56
BestRank
Statement
http://www.wikidata.org/entity/statement/Q22008704-3D1FA4E5-BBDC-4CA7-B237-43DCDCD0DC56
Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion-dependent carnitine transporter
P921
Q22008704-3D1FA4E5-BBDC-4CA7-B237-43DCDCD0DC56
BestRank
Statement
http://www.wikidata.org/entity/statement/Q22008704-3D1FA4E5-BBDC-4CA7-B237-43DCDCD0DC56
rank
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type
BestRank
Statement
wasDerivedFrom
17da9be1f8890cd10616e848aec6b571eb80d078
P921
Solute carrier family 22 member 5