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- NCIT_C190842 IAO_0000115 "Human SLC13A5 wild-type allele is located in the vicinity of 17p13.1 and is approximately 29 kb in length. This allele, which encodes Na(+)/citrate cotransporter protein, is involved in citrate transport. Mutation of the gene is associated with developmental and epileptic encephalopathy 25, with amelogenesis imperfecta." @default.
- NCIT_C190842 NCIT_NHC0 "C190842" @default.
- NCIT_C190842 NCIT_P100 "608305" @default.
- NCIT_C190842 NCIT_P102 "AJ489980" @default.
- NCIT_C190842 NCIT_P106 "Gene or Genome" @default.
- NCIT_C190842 NCIT_P108 "SLC13A5 wt Allele" @default.
- NCIT_C190842 NCIT_P208 "CL1799305" @default.
- NCIT_C190842 NCIT_P321 "284111" @default.
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- NCIT_C190842 NCIT_R41 NCIT_C25796 @default.
- NCIT_C190842 NCIT_R41 NCIT_C79740 @default.
- NCIT_C190842 normalizedInformationContent "100" @default.
- NCIT_C190842 referenceCount "1" @default.
- NCIT_C190842 hasExactSynonym "DEE25" @default.
- NCIT_C190842 hasExactSynonym "EIEE25" @default.
- NCIT_C190842 hasExactSynonym "INDY" @default.
- NCIT_C190842 hasExactSynonym "NACT" @default.
- NCIT_C190842 hasExactSynonym "SLC13A5 wt Allele" @default.
- NCIT_C190842 hasExactSynonym "Solute Carrier Family 13 (Sodium-Dependent Citrate Transporter), Member 5 Gene" @default.
- NCIT_C190842 hasExactSynonym "Solute Carrier Family 13 Member 5 wt Allele" @default.
- NCIT_C190842 hasExactSynonym "mIndy" @default.
- NCIT_C190842 type Class @default.
- NCIT_C190842 isDefinedBy ncit.owl @default.
- NCIT_C190842 label "SLC13A5 wt Allele" @default.
- NCIT_C190842 subClassOf Bbbb7c19627fbcbf4d858b3cced2e9b5a @default.
- NCIT_C190842 subClassOf Bcb612bf8fc3e243557056ef36b994a61 @default.
- NCIT_C190842 subClassOf NCIT_C16612 @default.
- NCIT_C190842 subClassOf NCIT_C190841 @default.
- NCIT_C190842 subClassOf NCIT_C190842 @default.
- NCIT_C190842 subClassOf NCIT_C21295 @default.
- NCIT_C190842 subClassOf NCIT_C28533 @default.