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
Q41897276-CD8A4018-A0C5-434B-BFCA-3A4084E11222
Q41897276-CD8A4018-A0C5-434B-BFCA-3A4084E11222
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41897276-CD8A4018-A0C5-434B-BFCA-3A4084E11222
Mutations in human lipoyltransferase gene LIPT1 cause a Leigh disease with secondary deficiency for pyruvate and alpha-ketoglutarate dehydrogenase.
P2860
Q41897276-CD8A4018-A0C5-434B-BFCA-3A4084E11222
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41897276-CD8A4018-A0C5-434B-BFCA-3A4084E11222
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
456baaec233362126d3e689c35400442711e4f25
P2860
Mutation of the iron-sulfur cluster assembly gene IBA57 causes severe myopathy and encephalopathy.