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Q28138497-9F1D0D1B-3918-4F17-9657-C360046E523D
Q28138497-9F1D0D1B-3918-4F17-9657-C360046E523D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28138497-9F1D0D1B-3918-4F17-9657-C360046E523D
Mutations of OCTN2, an organic cation/carnitine transporter, lead to deficient cellular carnitine uptake in primary carnitine deficiency
P2860
Q28138497-9F1D0D1B-3918-4F17-9657-C360046E523D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28138497-9F1D0D1B-3918-4F17-9657-C360046E523D
rank
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type
BestRank
Statement
wasDerivedFrom
138f134bf1bdecc6e51535c881cf463721788b6e
P2860
cDNA sequence, transport function, and genomic organization of human OCTN2, a new member of the organic cation transporter family