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Q34462269-30362C35-213A-466F-990D-F4D96BF44094
Q34462269-30362C35-213A-466F-990D-F4D96BF44094
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34462269-30362C35-213A-466F-990D-F4D96BF44094
Carnitine deficiency in OCTN2-/- newborn mice leads to a severe gut and immune phenotype with widespread atrophy, apoptosis and a pro-inflammatory response
P2860
Q34462269-30362C35-213A-466F-990D-F4D96BF44094
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34462269-30362C35-213A-466F-990D-F4D96BF44094
rank
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type
BestRank
Statement
wasDerivedFrom
f58919fe2304dd8160f89fde4d413bb7e33cc0b6
P2860
Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion-dependent carnitine transporter