Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C84413> ?p ?o ?g. }
Showing items 1 to 70 of
70
with 100 items per page.
- NCIT_C84413 IAO_0000115 "Human SIX1 wild-type allele is located in the vicinity of 14q23.1 and is approximately 3 kb in length. This allele, which encodes homeobox protein SIX1, may play a role in skeletal muscle development. Mutation of the gene is associated with both autosomal dominant deafness type 23 and branchiootic syndrome type 3." @default.
- NCIT_C84413 NCIT_NHC0 "C84413" @default.
- NCIT_C84413 NCIT_P100 "601205" @default.
- NCIT_C84413 NCIT_P102 "X91868" @default.
- NCIT_C84413 NCIT_P106 "Gene or Genome" @default.
- NCIT_C84413 NCIT_P107 "SIX1 wt Allele" @default.
- NCIT_C84413 NCIT_P108 "SIX1 wt Allele" @default.
- NCIT_C84413 NCIT_P207 "C2827437" @default.
- NCIT_C84413 NCIT_P321 "6495" @default.
- NCIT_C84413 NCIT_P322 "CTRP" @default.
- NCIT_C84413 NCIT_R37 NCIT_C16399 @default.
- NCIT_C84413 NCIT_R37 NCIT_C16879 @default.
- NCIT_C84413 NCIT_R37 NCIT_C17710 @default.
- NCIT_C84413 NCIT_R37 NCIT_C17729 @default.
- NCIT_C84413 NCIT_R37 NCIT_C17828 @default.
- NCIT_C84413 NCIT_R37 NCIT_C18219 @default.
- NCIT_C84413 NCIT_R37 NCIT_C18597 @default.
- NCIT_C84413 NCIT_R37 NCIT_C19077 @default.
- NCIT_C84413 NCIT_R37 NCIT_C19946 @default.
- NCIT_C84413 NCIT_R37 NCIT_C19970 @default.
- NCIT_C84413 NCIT_R37 NCIT_C19986 @default.
- NCIT_C84413 NCIT_R37 NCIT_C20480 @default.
- NCIT_C84413 NCIT_R37 NCIT_C21049 @default.
- NCIT_C84413 NCIT_R37 NCIT_C21050 @default.
- NCIT_C84413 NCIT_R37 NCIT_C21124 @default.
- NCIT_C84413 NCIT_R37 NCIT_C21147 @default.
- NCIT_C84413 NCIT_R37 NCIT_C28498 @default.
- NCIT_C84413 NCIT_R37 NCIT_C40523 @default.
- NCIT_C84413 NCIT_R40 NCIT_C12219 @default.
- NCIT_C84413 NCIT_R40 NCIT_C13282 @default.
- NCIT_C84413 NCIT_R40 NCIT_C13377 @default.
- NCIT_C84413 NCIT_R40 NCIT_C13432 @default.
- NCIT_C84413 NCIT_R40 NCIT_C13446 @default.
- NCIT_C84413 NCIT_R40 NCIT_C14135 @default.
- NCIT_C84413 NCIT_R40 NCIT_C32221 @default.
- NCIT_C84413 NCIT_R40 NCIT_C34070 @default.
- NCIT_C84413 NCIT_R40 NCIT_C54570 @default.
- NCIT_C84413 NCIT_R41 NCIT_C14182 @default.
- NCIT_C84413 NCIT_R41 NCIT_C14225 @default.
- NCIT_C84413 NCIT_R41 NCIT_C14234 @default.
- NCIT_C84413 NCIT_R41 NCIT_C14250 @default.
- NCIT_C84413 NCIT_R41 NCIT_C14262 @default.
- NCIT_C84413 NCIT_R41 NCIT_C14282 @default.
- NCIT_C84413 NCIT_R41 NCIT_C25796 @default.
- NCIT_C84413 NCIT_R41 NCIT_C79740 @default.
- NCIT_C84413 normalizedInformationContent "100" @default.
- NCIT_C84413 referenceCount "1" @default.
- NCIT_C84413 hasExactSynonym "BOS3" @default.
- NCIT_C84413 hasExactSynonym "DFNA23" @default.
- NCIT_C84413 hasExactSynonym "Deafness, Autosomal Dominant 23 Gene" @default.
- NCIT_C84413 hasExactSynonym "SIX Homeobox 1 wt Allele" @default.
- NCIT_C84413 hasExactSynonym "SIX1 wt Allele" @default.
- NCIT_C84413 hasExactSynonym "Sine Oculis Homeobox (Drosophila) Homolog 1 Gene" @default.
- NCIT_C84413 hasExactSynonym "Sine Oculis Homeobox Homolog 1 (Drosophila) Gene" @default.
- NCIT_C84413 hasExactSynonym "Sine Oculis Homeobox, Drosophila, Homolog of, 1 Gene" @default.
- NCIT_C84413 hasExactSynonym "TIP39" @default.
- NCIT_C84413 inSubset NCIT_C116977 @default.
- NCIT_C84413 inSubset NCIT_C142799 @default.
- NCIT_C84413 inSubset NCIT_C142800 @default.
- NCIT_C84413 type Class @default.
- NCIT_C84413 isDefinedBy ncit.owl @default.
- NCIT_C84413 label "SIX1 wt Allele" @default.
- NCIT_C84413 subClassOf B8c30edcbb839a6e72a20bb431add983c @default.
- NCIT_C84413 subClassOf Bef0823e6ac4a991d605cc3dda71f3a7a @default.
- NCIT_C84413 subClassOf NCIT_C16612 @default.
- NCIT_C84413 subClassOf NCIT_C16615 @default.
- NCIT_C84413 subClassOf NCIT_C20420 @default.
- NCIT_C84413 subClassOf NCIT_C54362 @default.
- NCIT_C84413 subClassOf NCIT_C84410 @default.
- NCIT_C84413 subClassOf NCIT_C84413 @default.