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- NCIT_C51707 IAO_0000115 "Human NR0B2 wild-type allele is located in the vicinity of 1p36.1 and is approximately 2 kb in length. This allele, which encodes nuclear receptor 0B2 protein, is involved in transcriptional repression that is mediated by nuclear hormone receptor interactions. Mutations and dysfunction in the gene is associated with obesity." @default.
- NCIT_C51707 NCIT_NHC0 "C51707" @default.
- NCIT_C51707 NCIT_P100 "604630" @default.
- NCIT_C51707 NCIT_P102 "NM_021969" @default.
- NCIT_C51707 NCIT_P106 "Gene or Genome" @default.
- NCIT_C51707 NCIT_P107 "NR0B2 wt Allele" @default.
- NCIT_C51707 NCIT_P108 "NR0B2 wt Allele" @default.
- NCIT_C51707 NCIT_P207 "C1705299" @default.
- NCIT_C51707 NCIT_P211 "cholesterol metabolism" @default.
- NCIT_C51707 NCIT_P211 "ligand-dependent nuclear receptor activity" @default.
- NCIT_C51707 NCIT_P211 "negative regulation of transcription from Pol II promoter" @default.
- NCIT_C51707 NCIT_P211 "nucleus" @default.
- NCIT_C51707 NCIT_P211 "transcription co-repressor activity" @default.
- NCIT_C51707 NCIT_P321 "8431" @default.
- NCIT_C51707 NCIT_P322 "CTRP" @default.
- NCIT_C51707 NCIT_P366 "NR0B2_wt_Allele" @default.
- NCIT_C51707 NCIT_P96 "Orphan Nuclear Receptor SHP" @default.
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- NCIT_C51707 normalizedInformationContent "100" @default.
- NCIT_C51707 referenceCount "1" @default.
- NCIT_C51707 hasExactSynonym "NR0B2 wt Allele" @default.
- NCIT_C51707 hasExactSynonym "NR0B2" @default.
- NCIT_C51707 hasExactSynonym "Nuclear Receptor Subfamily 0, Group B, Member 2 wt Allele" @default.
- NCIT_C51707 hasExactSynonym "SHP" @default.
- NCIT_C51707 hasExactSynonym "SHP1" @default.
- NCIT_C51707 inSubset NCIT_C116977 @default.
- NCIT_C51707 inSubset NCIT_C142799 @default.
- NCIT_C51707 inSubset NCIT_C142800 @default.
- NCIT_C51707 type Class @default.
- NCIT_C51707 isDefinedBy ncit.owl @default.
- NCIT_C51707 label "NR0B2 wt Allele" @default.
- NCIT_C51707 subClassOf NCIT_C16612 @default.
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