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Namespace Prefixes

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Statements

Subject Item

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n3:ECO_0007645

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n3:IAO_0000115

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An infancy electroclinical syndrome characterized by onset of focal seizures in infancy and exercise-induced dystonia in childhood that has_material_basis_in homozygous or compound heterozygous mutation in TBC1D24 on chromosome 16p13.3.

obo:hasDbXref

url:https://www.ncbi.nlm.nih.gov/pubmed/31257402