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Q35070259-E43DE649-C30B-4185-83A5-7C354AF72215
Q35070259-E43DE649-C30B-4185-83A5-7C354AF72215
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35070259-E43DE649-C30B-4185-83A5-7C354AF72215
Ophthalmological phenotype associated with homozygous null mutation in the NEUROD1 gene.
P1476
Q35070259-E43DE649-C30B-4185-83A5-7C354AF72215
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35070259-E43DE649-C30B-4185-83A5-7C354AF72215
rank
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wasDerivedFrom
abbff3ea209a748f79aa202858d43a24f4687dc0
P1476
Ophthalmological phenotype associated with homozygous null mutation in the NEUROD1 gene.
@en