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- NCIT_C162472 IAO_0000115 "An autosomal dominant form of early infantile epileptic encephalopathy, caused by mutation(s) in the STXBP1 gene, encoding syntaxin-binding protein 1." @default.
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- NCIT_C162472 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C162472 NCIT_P108 "Developmental and Epileptic Encephalopathy 4" @default.
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- NCIT_C162472 hasExactSynonym "DEE4" @default.
- NCIT_C162472 hasExactSynonym "Developmental and Epileptic Encephalopathy 4" @default.
- NCIT_C162472 hasExactSynonym "EIEE4" @default.
- NCIT_C162472 hasExactSynonym "Early Infantile Epileptic Encephalopathy 4" @default.
- NCIT_C162472 inSubset NCIT_C165258 @default.
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