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Q24307529-0888F05B-6C21-4F39-A0C9-332814385A45
Q24307529-0888F05B-6C21-4F39-A0C9-332814385A45
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24307529-0888F05B-6C21-4F39-A0C9-332814385A45
RP1L1 variants are associated with a spectrum of inherited retinal diseases including retinitis pigmentosa and occult macular dystrophy
P921
Q24307529-0888F05B-6C21-4F39-A0C9-332814385A45
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24307529-0888F05B-6C21-4F39-A0C9-332814385A45
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
17da9be1f8890cd10616e848aec6b571eb80d078
P921
Retinitis pigmentosa 1 (human)