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- NCIT_C177193 IAO_0000115 "Human ATP7B wild-type allele is located in the vicinity of 13q14.3 and is approximately 82 kb in length. This allele, which encodes copper-transporting ATPase 2 protein, is involved in copper ion homeostasis. Mutation of the gene is associated with Wilson disease." @default.
- NCIT_C177193 NCIT_NHC0 "C177193" @default.
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- NCIT_C177193 NCIT_P106 "Gene or Genome" @default.
- NCIT_C177193 NCIT_P108 "ATP7B wt Allele" @default.
- NCIT_C177193 NCIT_P208 "CL1643022" @default.
- NCIT_C177193 NCIT_P321 "540" @default.
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- NCIT_C177193 normalizedInformationContent "100" @default.
- NCIT_C177193 referenceCount "1" @default.
- NCIT_C177193 hasExactSynonym "ATP7B wt Allele" @default.
- NCIT_C177193 hasExactSynonym "ATPase Copper Transporting Beta wt Allele" @default.
- NCIT_C177193 hasExactSynonym "ATPase, Cu(2+)-Transporting, Beta Polypeptide Gene" @default.
- NCIT_C177193 hasExactSynonym "ATPase, Cu++ Transporting, Beta Polypeptide (Wilson Disease) Gene" @default.
- NCIT_C177193 hasExactSynonym "ATPase, Cu++ Transporting, Beta Polypeptide Gene" @default.
- NCIT_C177193 hasExactSynonym "PWD" @default.
- NCIT_C177193 hasExactSynonym "WC1" @default.
- NCIT_C177193 hasExactSynonym "WD" @default.
- NCIT_C177193 hasExactSynonym "WND" @default.
- NCIT_C177193 hasExactSynonym "Wilson Disease Gene" @default.
- NCIT_C177193 type Class @default.
- NCIT_C177193 isDefinedBy ncit.owl @default.
- NCIT_C177193 label "ATP7B wt Allele" @default.
- NCIT_C177193 subClassOf B35c8b17cba48e725c8dfcdaf9c05d6ea @default.
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- NCIT_C177193 subClassOf NCIT_C21281 @default.
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