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- NCIT_C175707 IAO_0000115 "A genetic condition associated with mutation(s) in the C19orf12 gene, encoding protein C19orf12. It is characterized by progressive spastic paraplegia, parkinsonism unresponsive to L-DOPA treatment, and psychiatric or behavioral symptoms." @default.
- NCIT_C175707 NCIT_NHC0 "C175707" @default.
- NCIT_C175707 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C175707 NCIT_P108 "Neurodegeneration with Brain Iron Accumulation 4" @default.
- NCIT_C175707 NCIT_P207 "C3280371" @default.
- NCIT_C175707 NCIT_P322 "Cellosaurus" @default.
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- NCIT_C175707 NCIT_R100 NCIT_C12919 @default.
- NCIT_C175707 NCIT_R100 NCIT_C13040 @default.
- NCIT_C175707 NCIT_R100 NCIT_C32221 @default.
- NCIT_C175707 NCIT_R176 NCIT_C16612 @default.
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- NCIT_C175707 hasExactSynonym "NBIA4" @default.
- NCIT_C175707 hasExactSynonym "Neurodegeneration With Brain Iron Accumulation 4" @default.
- NCIT_C175707 hasExactSynonym "Neurodegeneration with Brain Iron Accumulation 4" @default.
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- NCIT_C175707 type Class @default.
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- NCIT_C175707 label "Neurodegeneration with Brain Iron Accumulation 4" @default.
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