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2
Q28296223-BB3B20E3-BFEC-475D-B5E6-E996A552B23A
Q28296223-BB3B20E3-BFEC-475D-B5E6-E996A552B23A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28296223-BB3B20E3-BFEC-475D-B5E6-E996A552B23A
Leber congenital amaurosis caused by a homozygous mutation (R90W) in the homeodomain of the retinal transcription factor CRX: direct evidence for the involvement of CRX in the development of photoreceptor function
P2093
Q28296223-BB3B20E3-BFEC-475D-B5E6-E996A552B23A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28296223-BB3B20E3-BFEC-475D-B5E6-E996A552B23A
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
5c00672b58ee3f68b8d9df15d3b637342e780ab5
P1545
6
http://www.w3.org/2001/XMLSchema#string
P2093
S Xu
http://www.w3.org/2001/XMLSchema#string