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
Q26770321-3F2D0EAF-1466-4191-923C-8509F35910F9
Q26770321-3F2D0EAF-1466-4191-923C-8509F35910F9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q26770321-3F2D0EAF-1466-4191-923C-8509F35910F9
Retinal dystrophies, genomic applications in diagnosis and prospects for therapy
P2860
Q26770321-3F2D0EAF-1466-4191-923C-8509F35910F9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q26770321-3F2D0EAF-1466-4191-923C-8509F35910F9
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
ac3f9afd1a93e6ee50bcf14be81960b4be35c4d2
P2860
Mutations in the gene KCNV2 encoding a voltage-gated potassium channel subunit cause "cone dystrophy with supernormal rod electroretinogram" in humans