elhamkhani
/
Test2
/
Login
Register
TriplyDB
Test2
Browser
Table
SPARQL
Graphs
1
1
Services
1
1
Assets
0
0
Insights
Schema
BETA
Class frequency
Class hierarchy
Q22008704-B63ECE86-6EFA-4EEB-8ABA-25EDD1144573
Q22008704-B63ECE86-6EFA-4EEB-8ABA-25EDD1144573
BestRank
Statement
http://www.wikidata.org/entity/statement/Q22008704-B63ECE86-6EFA-4EEB-8ABA-25EDD1144573
Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion-dependent carnitine transporter
P2860
Q22008704-B63ECE86-6EFA-4EEB-8ABA-25EDD1144573
BestRank
Statement
http://www.wikidata.org/entity/statement/Q22008704-B63ECE86-6EFA-4EEB-8ABA-25EDD1144573
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
e953cef9d302ca1202c790b3d5554b44cbd946c0
P2860
Systemic carnitine deficiency--a treatable inherited lipid-storage disease presenting as Reye's syndrome.