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- NCIT_C186688 IAO_0000115 "Human MSH5 wild-type allele is located in the vicinity of 6p21.33 and is approximately 23 kb in length. This allele, which encodes MutS protein homolog 5 protein, is involved in meiotic recombination and DNA repair. Mutation of the gene is associated with premature ovarian failure 13 and may be associated with IgA deficiency or common variable immunodeficiency." @default.
- NCIT_C186688 NCIT_NHC0 "C186688" @default.
- NCIT_C186688 NCIT_P100 "603382" @default.
- NCIT_C186688 NCIT_P102 "AF070071" @default.
- NCIT_C186688 NCIT_P106 "Gene or Genome" @default.
- NCIT_C186688 NCIT_P108 "MSH5 wt Allele" @default.
- NCIT_C186688 NCIT_P208 "CL1779157" @default.
- NCIT_C186688 NCIT_P321 "4439" @default.
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- NCIT_C186688 NCIT_R41 NCIT_C25796 @default.
- NCIT_C186688 NCIT_R41 NCIT_C79740 @default.
- NCIT_C186688 normalizedInformationContent "100" @default.
- NCIT_C186688 referenceCount "1" @default.
- NCIT_C186688 hasExactSynonym "G7" @default.
- NCIT_C186688 hasExactSynonym "MSH5 wt Allele" @default.
- NCIT_C186688 hasExactSynonym "MUTSH5" @default.
- NCIT_C186688 hasExactSynonym "MutS (E. coli) Homolog 5 Gene" @default.
- NCIT_C186688 hasExactSynonym "MutS Homolog 4 wt Allele" @default.
- NCIT_C186688 hasExactSynonym "MutS Homolog 5 (E. coli) Gene" @default.
- NCIT_C186688 hasExactSynonym "MutS Homolog 5 wt Allele" @default.
- NCIT_C186688 hasExactSynonym "MutS, E. coli, Homolog of, 5 Gene" @default.
- NCIT_C186688 hasExactSynonym "NG23" @default.
- NCIT_C186688 hasExactSynonym "POF13" @default.
- NCIT_C186688 type Class @default.
- NCIT_C186688 isDefinedBy ncit.owl @default.
- NCIT_C186688 label "MSH5 wt Allele" @default.
- NCIT_C186688 subClassOf Ba9c20cca22681338b1035ffdb8f11c55 @default.
- NCIT_C186688 subClassOf Be47a0b492612daf5ed2d9a5688a55a46 @default.
- NCIT_C186688 subClassOf NCIT_C16612 @default.
- NCIT_C186688 subClassOf NCIT_C186687 @default.
- NCIT_C186688 subClassOf NCIT_C186688 @default.
- NCIT_C186688 subClassOf NCIT_C19676 @default.