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1
3280605
3280605
https://w3id.org/oc/corpus/br/3280605
FOXG1 is responsible for the congenital variant of Rett syndrome
P3181
d9eee132effd6b80840a6991a25b93b043fc2e5d
P3181
Q24647431-65219B39-D5D9-41CC-86A8-935E83CA3239
P3181
3280605
https://w3id.org/oc/corpus/br/3280605