awgldk
/
wikidata
/
Login
Register
TriplyDB
Wikidata
Browser
Table
SPARQL
Graphs
1
1
Services
1
1
Assets
0
0
Insights
Schema
BETA
Class frequency
Class hierarchy
Q42752301-3E9404B2-5629-4ACB-82EB-E5C6F3EC0CDE
Q42752301-3E9404B2-5629-4ACB-82EB-E5C6F3EC0CDE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42752301-3E9404B2-5629-4ACB-82EB-E5C6F3EC0CDE
Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome.
P2860
Q42752301-3E9404B2-5629-4ACB-82EB-E5C6F3EC0CDE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42752301-3E9404B2-5629-4ACB-82EB-E5C6F3EC0CDE
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
56adcb7110d106ae21481eaa621b2317250c8936
P2860
MKS1, encoding a component of the flagellar apparatus basal body proteome, is mutated in Meckel syndrome.