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1
Q51842731-C282C8B5-7FAD-4967-B37E-9E7DC086461B
Q51842731-C282C8B5-7FAD-4967-B37E-9E7DC086461B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51842731-C282C8B5-7FAD-4967-B37E-9E7DC086461B
Congenital hypothyroidism caused by a novel homozygous mutation in the thyroid peroxidase gene.
P2093
Q51842731-C282C8B5-7FAD-4967-B37E-9E7DC086461B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51842731-C282C8B5-7FAD-4967-B37E-9E7DC086461B
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
29933acc505ea44009015f0d67e19007e135f3ee
P1545
1
http://www.w3.org/2001/XMLSchema#string
P2093
Fuchs O
http://www.w3.org/2001/XMLSchema#string