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- NCIT_C128927 IAO_0000115 "Human DLX5 wild-type allele is located in the vicinity of 7q21.3 and is approximately 5 kb in length. This allele, which encodes homeobox protein DLX-5, plays a role in transcriptional activation that is essential for osteoblast differentiation. Mutation of the gene is associated with split-hand/foot malformation 1 with sensorineural hearing loss." @default.
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- NCIT_C128927 NCIT_P106 "Gene or Genome" @default.
- NCIT_C128927 NCIT_P107 "DLX5 wt Allele" @default.
- NCIT_C128927 NCIT_P108 "DLX5 wt Allele" @default.
- NCIT_C128927 NCIT_P208 "CL512130" @default.
- NCIT_C128927 NCIT_P321 "1749" @default.
- NCIT_C128927 NCIT_P322 "CTRP" @default.
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- NCIT_C128927 normalizedInformationContent "100" @default.
- NCIT_C128927 referenceCount "1" @default.
- NCIT_C128927 hasExactSynonym "DLX5 wt Allele" @default.
- NCIT_C128927 hasExactSynonym "Distal-Less Homeo Box 5 Gene" @default.
- NCIT_C128927 hasExactSynonym "Distal-Less Homeobox 5 wt Allele" @default.
- NCIT_C128927 hasExactSynonym "SHFM1D" @default.
- NCIT_C128927 hasExactSynonym "Split Hand/Foot Malformation Type 1 With Sensorineural Hearing Loss Gene" @default.
- NCIT_C128927 inSubset NCIT_C116977 @default.
- NCIT_C128927 inSubset NCIT_C142799 @default.
- NCIT_C128927 inSubset NCIT_C142800 @default.
- NCIT_C128927 type Class @default.
- NCIT_C128927 isDefinedBy ncit.owl @default.
- NCIT_C128927 label "DLX5 wt Allele" @default.
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