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- NCIT_C104564 IAO_0000115 "Human NCF2 wild-type allele is located in the vicinity of 1q25 and is approximately 35 kb in length. This allele, which encodes neutrophil cytosol factor 2 protein, is involved in the generation of superoxide in neutrophils. Mutations in this gene are associated with chronic granulomatous disease." @default.
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- NCIT_C104564 NCIT_P106 "Gene or Genome" @default.
- NCIT_C104564 NCIT_P107 "NCF2 wt Allele" @default.
- NCIT_C104564 NCIT_P108 "NCF2 wt Allele" @default.
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- NCIT_C104564 NCIT_P98 "Alternative splicing results in multiple transcript variants encoding different isoforms." @default.
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- NCIT_C104564 referenceCount "1" @default.
- NCIT_C104564 hasExactSynonym "Chronic Granulomatous Disease, Autosomal 2 Gene" @default.
- NCIT_C104564 hasExactSynonym "NCF-2" @default.
- NCIT_C104564 hasExactSynonym "NCF2 wt Allele" @default.
- NCIT_C104564 hasExactSynonym "NOXA2" @default.
- NCIT_C104564 hasExactSynonym "Neutrophil Cytosolic Factor 2 (65kD, Chronic Granulomatous Disease, Autosomal 2) Gene" @default.
- NCIT_C104564 hasExactSynonym "Neutrophil Cytosolic Factor 2 wt Allele" @default.
- NCIT_C104564 hasExactSynonym "P67-PHOX" @default.
- NCIT_C104564 hasExactSynonym "P67PHOX" @default.
- NCIT_C104564 hasExactSynonym "p67 PHOX" @default.
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- NCIT_C104564 type Class @default.
- NCIT_C104564 isDefinedBy ncit.owl @default.
- NCIT_C104564 label "NCF2 wt Allele" @default.
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