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- NCIT_C75880 IAO_0000115 "Human OFD1 wild-type allele is located in the vicinity of Xp22 and is approximately 35 kb in length. This allele, which encodes oral-facial-digital syndrome 1, may be involved in the mediation of embryonic development. Mutations in the gene are associated with both oral-facial-digital syndrome type I and Simpson-Golabi-Behmel syndrome type 2." @default.
- NCIT_C75880 NCIT_NHC0 "C75880" @default.
- NCIT_C75880 NCIT_P100 "300170" @default.
- NCIT_C75880 NCIT_P102 "Y15164" @default.
- NCIT_C75880 NCIT_P106 "Gene or Genome" @default.
- NCIT_C75880 NCIT_P107 "OFD1 wt Allele" @default.
- NCIT_C75880 NCIT_P108 "OFD1 wt Allele" @default.
- NCIT_C75880 NCIT_P207 "C2698641" @default.
- NCIT_C75880 NCIT_P321 "8481" @default.
- NCIT_C75880 NCIT_P322 "CTRP" @default.
- NCIT_C75880 NCIT_P366 "OFD1_wt_Allele" @default.
- NCIT_C75880 NCIT_P98 "Several OFD1 pseudogenes are in the human genome, one is located on chromosome 5 and at least sixteen have been found in a cluster on the Y chromosome in the vicinity of Yp11. (Entrez Gene and HUGO)" @default.
- NCIT_C75880 NCIT_R40 NCIT_C12219 @default.
- NCIT_C75880 NCIT_R40 NCIT_C13282 @default.
- NCIT_C75880 NCIT_R40 NCIT_C13377 @default.
- NCIT_C75880 NCIT_R40 NCIT_C13432 @default.
- NCIT_C75880 NCIT_R40 NCIT_C13446 @default.
- NCIT_C75880 NCIT_R40 NCIT_C14135 @default.
- NCIT_C75880 NCIT_R40 NCIT_C25138 @default.
- NCIT_C75880 NCIT_R40 NCIT_C32221 @default.
- NCIT_C75880 NCIT_R40 NCIT_C34070 @default.
- NCIT_C75880 NCIT_R41 NCIT_C14182 @default.
- NCIT_C75880 NCIT_R41 NCIT_C14225 @default.
- NCIT_C75880 NCIT_R41 NCIT_C14234 @default.
- NCIT_C75880 NCIT_R41 NCIT_C14250 @default.
- NCIT_C75880 NCIT_R41 NCIT_C14262 @default.
- NCIT_C75880 NCIT_R41 NCIT_C14282 @default.
- NCIT_C75880 NCIT_R41 NCIT_C25796 @default.
- NCIT_C75880 NCIT_R41 NCIT_C79740 @default.
- NCIT_C75880 normalizedInformationContent "100" @default.
- NCIT_C75880 referenceCount "1" @default.
- NCIT_C75880 hasExactSynonym "71-7A" @default.
- NCIT_C75880 hasExactSynonym "CXorf5" @default.
- NCIT_C75880 hasExactSynonym "Chromosome X Open Reading Frame 5 Gene" @default.
- NCIT_C75880 hasExactSynonym "JBTS10" @default.
- NCIT_C75880 hasExactSynonym "MGC117039" @default.
- NCIT_C75880 hasExactSynonym "MGC117040" @default.
- NCIT_C75880 hasExactSynonym "OFD1 wt Allele" @default.
- NCIT_C75880 hasExactSynonym "Oral-Facial-Digital Syndrome 1 wt Allele" @default.
- NCIT_C75880 hasExactSynonym "Retinitis Pigmentosa 23 (X-Linked Recessive) Gene" @default.
- NCIT_C75880 hasExactSynonym "SGBS2" @default.
- NCIT_C75880 inSubset NCIT_C116977 @default.
- NCIT_C75880 inSubset NCIT_C142799 @default.
- NCIT_C75880 inSubset NCIT_C142800 @default.
- NCIT_C75880 type Class @default.
- NCIT_C75880 isDefinedBy ncit.owl @default.
- NCIT_C75880 label "OFD1 wt Allele" @default.
- NCIT_C75880 subClassOf B11ce546d3b991ae0f58ac455a1a32d11 @default.
- NCIT_C75880 subClassOf B586694611fa82d2a16d644fca06260ff @default.
- NCIT_C75880 subClassOf B9806d9375a95e2e36b54a20a78028f32 @default.
- NCIT_C75880 subClassOf Be4014b3f2e8048ee40e3d8c16c34287a @default.
- NCIT_C75880 subClassOf NCIT_C16612 @default.
- NCIT_C75880 subClassOf NCIT_C20194 @default.
- NCIT_C75880 subClassOf NCIT_C75879 @default.
- NCIT_C75880 subClassOf NCIT_C75880 @default.