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- NCIT_C74448 IAO_0000115 "Human NOD2 wild-type allele is located in the vicinity of 16q21 and is approximately 36 kb in length. This allele, which encodes nucleotide-binding oligomerization domain-containing protein 2, plays a role in the modulation of both cell death and immune response. Mutation of the gene is associated with Blau syndrome, Crohn disease, ulcerative colitis, and early-onset sarcoidosis." @default.
- NCIT_C74448 NCIT_NHC0 "C74448" @default.
- NCIT_C74448 NCIT_P100 "605956" @default.
- NCIT_C74448 NCIT_P102 "AF178930" @default.
- NCIT_C74448 NCIT_P106 "Gene or Genome" @default.
- NCIT_C74448 NCIT_P108 "NOD2 wt Allele" @default.
- NCIT_C74448 NCIT_P207 "C2698415" @default.
- NCIT_C74448 NCIT_P321 "64127" @default.
- NCIT_C74448 NCIT_P366 "NOD2_wt_Allele" @default.
- NCIT_C74448 NCIT_P98 "The NOD2 gene product interacts with the RIPK2 gene product. (SwissProt)" @default.
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- NCIT_C74448 hasExactSynonym "ACUG" @default.
- NCIT_C74448 hasExactSynonym "BLAU" @default.
- NCIT_C74448 hasExactSynonym "CARD15" @default.
- NCIT_C74448 hasExactSynonym "CD" @default.
- NCIT_C74448 hasExactSynonym "CLR16.3" @default.
- NCIT_C74448 hasExactSynonym "IBD1" @default.
- NCIT_C74448 hasExactSynonym "NLRC2" @default.
- NCIT_C74448 hasExactSynonym "NOD2 wt Allele" @default.
- NCIT_C74448 hasExactSynonym "NOD2B" @default.
- NCIT_C74448 hasExactSynonym "Nucleotide-Binding Oligomerization Domain Containing 2 wt Allele" @default.
- NCIT_C74448 hasExactSynonym "PSORAS1" @default.
- NCIT_C74448 type Class @default.
- NCIT_C74448 isDefinedBy ncit.owl @default.
- NCIT_C74448 label "NOD2 wt Allele" @default.
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- NCIT_C74448 subClassOf NCIT_C16612 @default.
- NCIT_C74448 subClassOf NCIT_C20462 @default.
- NCIT_C74448 subClassOf NCIT_C74447 @default.
- NCIT_C74448 subClassOf NCIT_C74448 @default.