wikimedia
/
wikidata
/
Login
Register
TriplyDB
Wikidata
Browser
Table
SPARQL
Graphs
1
1
Services
1
1
Assets
0
0
Insights
Schema
BETA
Class frequency
Class hierarchy
Q24657612-C0C9580B-38AB-4AA3-AAB0-F092D338D04A
Q24657612-C0C9580B-38AB-4AA3-AAB0-F092D338D04A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24657612-C0C9580B-38AB-4AA3-AAB0-F092D338D04A
Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome
P2860
Q24657612-C0C9580B-38AB-4AA3-AAB0-F092D338D04A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24657612-C0C9580B-38AB-4AA3-AAB0-F092D338D04A
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
ac2c941349c8ada8267edad6c4f2a433e878e838
P2860
The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules