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Q35070259-7FD854C4-7251-4AF2-ADB0-39B6A5D2F926
Q35070259-7FD854C4-7251-4AF2-ADB0-39B6A5D2F926
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35070259-7FD854C4-7251-4AF2-ADB0-39B6A5D2F926
Ophthalmological phenotype associated with homozygous null mutation in the NEUROD1 gene.
P932
Q35070259-7FD854C4-7251-4AF2-ADB0-39B6A5D2F926
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35070259-7FD854C4-7251-4AF2-ADB0-39B6A5D2F926
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
884fd24367d5a5c3e3ca16a30872d97429129ff3
P932
4323689
http://www.w3.org/2001/XMLSchema#string