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
Q35766412-28C0069E-BB12-478D-943F-0D78326D1DF4
Q35766412-28C0069E-BB12-478D-943F-0D78326D1DF4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35766412-28C0069E-BB12-478D-943F-0D78326D1DF4
Alu-mediated diverse and complex pathogenic copy-number variants within human chromosome 17 at p13.3.
P2860
Q35766412-28C0069E-BB12-478D-943F-0D78326D1DF4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35766412-28C0069E-BB12-478D-943F-0D78326D1DF4
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
ccf23ccdb9dddd3311f81fc50435cb45131a6f0b
P2860
Recurrent HERV-H-mediated 3q13.2-q13.31 deletions cause a syndrome of hypotonia and motor, language, and cognitive delays.