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- NCIT_C115180 IAO_0000115 "Human PPIB wild-type allele is located within 15q21-q22 and is approximately 7 kb in length. This allele, which encodes peptidyl-prolyl cis-trans isomerase B protein, is involved in protein folding. Mutation of the gene is associated with osteogenesis imperfecta type 9." @default.
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- NCIT_C115180 NCIT_P107 "PPIB wt Allele" @default.
- NCIT_C115180 NCIT_P108 "PPIB wt Allele" @default.
- NCIT_C115180 NCIT_P207 "C3890723" @default.
- NCIT_C115180 NCIT_P321 "5479" @default.
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- NCIT_C115180 hasExactSynonym "CYP-S1" @default.
- NCIT_C115180 hasExactSynonym "CYPB" @default.
- NCIT_C115180 hasExactSynonym "HEL-S-39" @default.
- NCIT_C115180 hasExactSynonym "OI9" @default.
- NCIT_C115180 hasExactSynonym "PPIB wt Allele" @default.
- NCIT_C115180 hasExactSynonym "Peptidylprolyl Isomerase B (Cyclophilin B) wt Allele" @default.
- NCIT_C115180 hasExactSynonym "SCYLP" @default.
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- NCIT_C115180 type Class @default.
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- NCIT_C115180 label "PPIB wt Allele" @default.
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