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
Q24671994-C1A05E91-25E1-4DB8-A9BE-B772BDBE81A1
Q24671994-C1A05E91-25E1-4DB8-A9BE-B772BDBE81A1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24671994-C1A05E91-25E1-4DB8-A9BE-B772BDBE81A1
The odyssey of MeCP2 and parental imprinting
P2860
Q24671994-C1A05E91-25E1-4DB8-A9BE-B772BDBE81A1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24671994-C1A05E91-25E1-4DB8-A9BE-B772BDBE81A1
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
dc152513090b769b6811dbe2fb7c623c6c1366e4
P2860
MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression