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- NCIT_C162631 IAO_0000115 "Human HOXB1 wild-type allele is located in the vicinity of 17q21.32 and is approximately 2 kb in length. This allele, which encodes homeobox protein Hox-B1, plays a role in the the regulation of anterior-posterior axis polarity. Mutation of the gene is associated with hereditary congenital facial palsy 3." @default.
- NCIT_C162631 NCIT_NHC0 "C162631" @default.
- NCIT_C162631 NCIT_P100 "142968" @default.
- NCIT_C162631 NCIT_P102 "NM_002144" @default.
- NCIT_C162631 NCIT_P106 "Gene or Genome" @default.
- NCIT_C162631 NCIT_P108 "HOXB1 wt Allele" @default.
- NCIT_C162631 NCIT_P208 "CL971016" @default.
- NCIT_C162631 NCIT_P321 "3211" @default.
- NCIT_C162631 NCIT_R37 NCIT_C16399 @default.
- NCIT_C162631 NCIT_R37 NCIT_C16879 @default.
- NCIT_C162631 NCIT_R37 NCIT_C17710 @default.
- NCIT_C162631 NCIT_R37 NCIT_C17828 @default.
- NCIT_C162631 NCIT_R37 NCIT_C18219 @default.
- NCIT_C162631 NCIT_R37 NCIT_C18597 @default.
- NCIT_C162631 NCIT_R37 NCIT_C19077 @default.
- NCIT_C162631 NCIT_R37 NCIT_C19970 @default.
- NCIT_C162631 NCIT_R37 NCIT_C19986 @default.
- NCIT_C162631 NCIT_R37 NCIT_C20480 @default.
- NCIT_C162631 NCIT_R37 NCIT_C21049 @default.
- NCIT_C162631 NCIT_R37 NCIT_C21050 @default.
- NCIT_C162631 NCIT_R37 NCIT_C21124 @default.
- NCIT_C162631 NCIT_R37 NCIT_C21147 @default.
- NCIT_C162631 NCIT_R37 NCIT_C28498 @default.
- NCIT_C162631 NCIT_R37 NCIT_C40523 @default.
- NCIT_C162631 NCIT_R40 NCIT_C12219 @default.
- NCIT_C162631 NCIT_R40 NCIT_C13282 @default.
- NCIT_C162631 NCIT_R40 NCIT_C13377 @default.
- NCIT_C162631 NCIT_R40 NCIT_C13432 @default.
- NCIT_C162631 NCIT_R40 NCIT_C13446 @default.
- NCIT_C162631 NCIT_R40 NCIT_C14135 @default.
- NCIT_C162631 NCIT_R40 NCIT_C32221 @default.
- NCIT_C162631 NCIT_R40 NCIT_C34070 @default.
- NCIT_C162631 NCIT_R40 NCIT_C38943 @default.
- NCIT_C162631 NCIT_R41 NCIT_C14182 @default.
- NCIT_C162631 NCIT_R41 NCIT_C14225 @default.
- NCIT_C162631 NCIT_R41 NCIT_C14234 @default.
- NCIT_C162631 NCIT_R41 NCIT_C14250 @default.
- NCIT_C162631 NCIT_R41 NCIT_C14262 @default.
- NCIT_C162631 NCIT_R41 NCIT_C14282 @default.
- NCIT_C162631 NCIT_R41 NCIT_C25796 @default.
- NCIT_C162631 NCIT_R41 NCIT_C79740 @default.
- NCIT_C162631 normalizedInformationContent "100" @default.
- NCIT_C162631 referenceCount "1" @default.
- NCIT_C162631 hasExactSynonym "HCFP3" @default.
- NCIT_C162631 hasExactSynonym "HOX2" @default.
- NCIT_C162631 hasExactSynonym "HOX2I" @default.
- NCIT_C162631 hasExactSynonym "HOXB1 wt Allele" @default.
- NCIT_C162631 hasExactSynonym "Homeo Box B1 Gene" @default.
- NCIT_C162631 hasExactSynonym "Homeobox 2I Gene" @default.
- NCIT_C162631 hasExactSynonym "Homeobox B1 wt Allele" @default.
- NCIT_C162631 hasExactSynonym "Hox-2.9" @default.
- NCIT_C162631 hasExactSynonym "Hox-2.9, Mouse, Homolog of Gene" @default.
- NCIT_C162631 type Class @default.
- NCIT_C162631 isDefinedBy ncit.owl @default.
- NCIT_C162631 label "HOXB1 wt Allele" @default.
- NCIT_C162631 subClassOf B653eb62ee7393a29a5cf600de346b80f @default.
- NCIT_C162631 subClassOf Bf32b9766295bf9c924875fcafbc49a25 @default.
- NCIT_C162631 subClassOf NCIT_C105822 @default.
- NCIT_C162631 subClassOf NCIT_C162630 @default.
- NCIT_C162631 subClassOf NCIT_C162631 @default.
- NCIT_C162631 subClassOf NCIT_C16612 @default.
- NCIT_C162631 subClassOf NCIT_C16615 @default.
- NCIT_C162631 subClassOf NCIT_C20420 @default.
- NCIT_C162631 subClassOf NCIT_C54362 @default.