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Q50133432-2A9F956A-AD3A-47F5-BA0B-AEE42121E881
Q50133432-2A9F956A-AD3A-47F5-BA0B-AEE42121E881
BestRank
Statement
http://www.wikidata.org/entity/statement/Q50133432-2A9F956A-AD3A-47F5-BA0B-AEE42121E881
Kallmann syndrome: phenotype and genotype of hypogonadotropic hypogonadism.
P2860
Q50133432-2A9F956A-AD3A-47F5-BA0B-AEE42121E881
BestRank
Statement
http://www.wikidata.org/entity/statement/Q50133432-2A9F956A-AD3A-47F5-BA0B-AEE42121E881
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
cd9409a8bbb38ebf7539c0e4bb5303e9944613fe
P2860
Functionally compromised CHD7 alleles in patients with isolated GnRH deficiency.