awgldk
/
wikidata
/
Login
Register
TriplyDB
Wikidata
Browser
Triples
Insights
Schema
BETA
Class frequency
Class hierarchy
SPARQL
Graphs
1
Q36765813-A5354740-4656-4591-9ED8-DC83AE33C23D
Q36765813-A5354740-4656-4591-9ED8-DC83AE33C23D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36765813-A5354740-4656-4591-9ED8-DC83AE33C23D
Mutation in collagen II alpha 1 isoforms delineates Stickler and Wagner syndrome phenotypes.
P2860
Q36765813-A5354740-4656-4591-9ED8-DC83AE33C23D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36765813-A5354740-4656-4591-9ED8-DC83AE33C23D
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
50c57cd7eff4f1166d9a90fefe4e46a0cf374083
P2860
A loss of function mutation in the COL9A2 gene causes autosomal recessive Stickler syndrome.