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- NCIT_C105836 IAO_0000115 "Human ATP5F1E wild-type allele is located in the vicinity of 20q13.32 and is approximately 7 kb in length. This allele, which encodes ATP synthase subunit epsilon, mitochondrial protein, plays a role in ATP biosynthesis. Mutation of the gene is associated with mitochondrial complex V (ATP synthase) deficiency nuclear type 3." @default.
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- NCIT_C105836 NCIT_P106 "Gene or Genome" @default.
- NCIT_C105836 NCIT_P107 "ATP5E wt Allele" @default.
- NCIT_C105836 NCIT_P108 "ATP5F1E wt Allele" @default.
- NCIT_C105836 NCIT_P207 "C3812228" @default.
- NCIT_C105836 NCIT_P321 "514" @default.
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- NCIT_C105836 normalizedInformationContent "100" @default.
- NCIT_C105836 referenceCount "1" @default.
- NCIT_C105836 hasExactSynonym "ATP Synthase F1 Subunit Epsilon wt Allele" @default.
- NCIT_C105836 hasExactSynonym "ATP Synthase, H+ Transporting, Mitochondrial F1 Complex, Epsilon Subunit Gene" @default.
- NCIT_C105836 hasExactSynonym "ATP5E wt Allele" @default.
- NCIT_C105836 hasExactSynonym "ATP5E" @default.
- NCIT_C105836 hasExactSynonym "ATP5F1E wt Allele" @default.
- NCIT_C105836 hasExactSynonym "ATPE" @default.
- NCIT_C105836 hasExactSynonym "MC5DN3" @default.
- NCIT_C105836 inSubset NCIT_C116977 @default.
- NCIT_C105836 inSubset NCIT_C142799 @default.
- NCIT_C105836 inSubset NCIT_C142800 @default.
- NCIT_C105836 type Class @default.
- NCIT_C105836 isDefinedBy ncit.owl @default.
- NCIT_C105836 label "ATP5F1E wt Allele" @default.
- NCIT_C105836 subClassOf NCIT_C105835 @default.
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- NCIT_C105836 subClassOf NCIT_C16612 @default.
- NCIT_C105836 subClassOf NCIT_C20194 @default.
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