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- NCIT_C107626 IAO_0000115 "Human KRT13 wild-type allele is located in the vicinity of 17q21.2 and is approximately 5 kb in length. This allele, which encodes keratin, type I cytoskeletal 13 protein, plays a role in epidermal development. Mutation of the gene is associated with white sponge nevus." @default.
- NCIT_C107626 NCIT_NHC0 "C107626" @default.
- NCIT_C107626 NCIT_P100 "148065" @default.
- NCIT_C107626 NCIT_P102 "NM_153490" @default.
- NCIT_C107626 NCIT_P106 "Gene or Genome" @default.
- NCIT_C107626 NCIT_P107 "KRT13 wt Allele" @default.
- NCIT_C107626 NCIT_P108 "KRT13 wt Allele" @default.
- NCIT_C107626 NCIT_P207 "C3810567" @default.
- NCIT_C107626 NCIT_P321 "3860" @default.
- NCIT_C107626 NCIT_P322 "CTRP" @default.
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- NCIT_C107626 normalizedInformationContent "100" @default.
- NCIT_C107626 referenceCount "1" @default.
- NCIT_C107626 hasExactSynonym "CK13" @default.
- NCIT_C107626 hasExactSynonym "K13" @default.
- NCIT_C107626 hasExactSynonym "KRT13 wt Allele" @default.
- NCIT_C107626 hasExactSynonym "Keratin 13 wt Allele" @default.
- NCIT_C107626 hasExactSynonym "MGC161462" @default.
- NCIT_C107626 hasExactSynonym "MGC3781" @default.
- NCIT_C107626 inSubset NCIT_C116977 @default.
- NCIT_C107626 inSubset NCIT_C142799 @default.
- NCIT_C107626 inSubset NCIT_C142800 @default.
- NCIT_C107626 type Class @default.
- NCIT_C107626 isDefinedBy ncit.owl @default.
- NCIT_C107626 label "KRT13 wt Allele" @default.
- NCIT_C107626 subClassOf Bbd8b08549a21e2d56028dfdf66be81ec @default.
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- NCIT_C107626 subClassOf NCIT_C16612 @default.
- NCIT_C107626 subClassOf NCIT_C20744 @default.
- NCIT_C107626 subClassOf NCIT_C20745 @default.
- NCIT_C107626 subClassOf NCIT_C30073 @default.