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
Q53522792-C8A52778-CDC6-47BB-B682-47E42B34A648
Q53522792-C8A52778-CDC6-47BB-B682-47E42B34A648
BestRank
Statement
http://www.wikidata.org/entity/statement/Q53522792-C8A52778-CDC6-47BB-B682-47E42B34A648
De novo SHANK3 mutation causes Rett syndrome-like phenotype in a female patient.
P2860
Q53522792-C8A52778-CDC6-47BB-B682-47E42B34A648
BestRank
Statement
http://www.wikidata.org/entity/statement/Q53522792-C8A52778-CDC6-47BB-B682-47E42B34A648
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
d11cbd7d98c81e930571d30dc4ddfe3d5217b3e0
P2860
SHANK3 as an autism spectrum disorder-associated gene.