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Q38290368-7B680165-CFB0-4B0F-BED2-E39ABA6B8B2D
Q38290368-7B680165-CFB0-4B0F-BED2-E39ABA6B8B2D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38290368-7B680165-CFB0-4B0F-BED2-E39ABA6B8B2D
Two mutations in the promoter region of the human protein C gene both cause type I protein C deficiency by disruption of two HNF-3 binding sites.
P2093
Q38290368-7B680165-CFB0-4B0F-BED2-E39ABA6B8B2D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38290368-7B680165-CFB0-4B0F-BED2-E39ABA6B8B2D
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
d2c77673586267f303d2f9afe02cf8833664d016
P1545
1
http://www.w3.org/2001/XMLSchema#string
P2093
Spek CA
http://www.w3.org/2001/XMLSchema#string