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Q33998365-2D604C6E-14AF-449B-A216-BE38C6602D1B
Q33998365-2D604C6E-14AF-449B-A216-BE38C6602D1B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33998365-2D604C6E-14AF-449B-A216-BE38C6602D1B
The retinal pigment epithelium in health and disease
P2860
Q33998365-2D604C6E-14AF-449B-A216-BE38C6602D1B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33998365-2D604C6E-14AF-449B-A216-BE38C6602D1B
rank
NormalRank
type
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Statement
wasDerivedFrom
a35cf40e963fc434e870ce92c6e9a800939a63e6
P2860
Retinal dystrophy due to paternal isodisomy for chromosome 1 or chromosome 2, with homoallelism for mutations in RPE65 or MERTK, respectively