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Q52586106-1A755795-3558-4C6A-B846-E96F1D9D1FB1
Q52586106-1A755795-3558-4C6A-B846-E96F1D9D1FB1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52586106-1A755795-3558-4C6A-B846-E96F1D9D1FB1
Special Issue Introduction: Inherited Retinal Disease: Novel Candidate Genes, Genotype-Phenotype Correlations, and Inheritance Models.
P2860
Q52586106-1A755795-3558-4C6A-B846-E96F1D9D1FB1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52586106-1A755795-3558-4C6A-B846-E96F1D9D1FB1
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
1dfb8f4d9f037c65ec3e6965e476478fc7d0a0ea
P2860
An initiator codon mutation in ornithine-delta-aminotransferase causing gyrate atrophy of the choroid and retina.