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
Q28583305-263805CE-748D-4A51-A931-0E4C0AE22A0E
Q28583305-263805CE-748D-4A51-A931-0E4C0AE22A0E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28583305-263805CE-748D-4A51-A931-0E4C0AE22A0E
Molecular phenotype of Fragile X syndrome: FMRP, FXRPs, and protein targets
P2860
Q28583305-263805CE-748D-4A51-A931-0E4C0AE22A0E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28583305-263805CE-748D-4A51-A931-0E4C0AE22A0E
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
11d0c82f45149d2f5e942c06de58985a81e27bd4
P2860
A point mutation in the FMR-1 gene associated with fragile X mental retardation.