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- NCIT_C101662 IAO_0000115 "Human TMEM216 wild-type allele is located in the vicinity of 11q13.1 and is approximately 7 kb in length. This allele, which encodes transmembrane protein 216, plays a role in the formation of cilium. Mutation of the gene is associated with Joubert syndrome type 2 and Meckel syndrome type 2." @default.
- NCIT_C101662 NCIT_NHC0 "C101662" @default.
- NCIT_C101662 NCIT_P100 "613277" @default.
- NCIT_C101662 NCIT_P102 "NM_001173991" @default.
- NCIT_C101662 NCIT_P106 "Gene or Genome" @default.
- NCIT_C101662 NCIT_P108 "TMEM216 wt Allele" @default.
- NCIT_C101662 NCIT_P207 "C3538789" @default.
- NCIT_C101662 NCIT_P321 "51259" @default.
- NCIT_C101662 NCIT_R37 NCIT_C17828 @default.
- NCIT_C101662 NCIT_R37 NCIT_C20480 @default.
- NCIT_C101662 NCIT_R37 NCIT_C26114 @default.
- NCIT_C101662 NCIT_R37 NCIT_C40792 @default.
- NCIT_C101662 NCIT_R40 NCIT_C12219 @default.
- NCIT_C101662 NCIT_R40 NCIT_C13282 @default.
- NCIT_C101662 NCIT_R40 NCIT_C13377 @default.
- NCIT_C101662 NCIT_R40 NCIT_C13432 @default.
- NCIT_C101662 NCIT_R40 NCIT_C13446 @default.
- NCIT_C101662 NCIT_R40 NCIT_C13876 @default.
- NCIT_C101662 NCIT_R40 NCIT_C14135 @default.
- NCIT_C101662 NCIT_R40 NCIT_C32221 @default.
- NCIT_C101662 NCIT_R40 NCIT_C34070 @default.
- NCIT_C101662 NCIT_R41 NCIT_C14182 @default.
- NCIT_C101662 NCIT_R41 NCIT_C14225 @default.
- NCIT_C101662 NCIT_R41 NCIT_C14234 @default.
- NCIT_C101662 NCIT_R41 NCIT_C14250 @default.
- NCIT_C101662 NCIT_R41 NCIT_C14262 @default.
- NCIT_C101662 NCIT_R41 NCIT_C14282 @default.
- NCIT_C101662 NCIT_R41 NCIT_C25796 @default.
- NCIT_C101662 NCIT_R41 NCIT_C79740 @default.
- NCIT_C101662 normalizedInformationContent "100" @default.
- NCIT_C101662 referenceCount "1" @default.
- NCIT_C101662 hasExactSynonym "Cerebello-Oculo-Renal Syndrome 2 Gene" @default.
- NCIT_C101662 hasExactSynonym "HSPC244" @default.
- NCIT_C101662 hasExactSynonym "JBTS2" @default.
- NCIT_C101662 hasExactSynonym "MGC13379" @default.
- NCIT_C101662 hasExactSynonym "MKS2" @default.
- NCIT_C101662 hasExactSynonym "Meckel Syndrome, Type 2 Gene" @default.
- NCIT_C101662 hasExactSynonym "TMEM216 wt Allele" @default.
- NCIT_C101662 hasExactSynonym "Transmembrane Protein 216 wt Allele" @default.
- NCIT_C101662 type Class @default.
- NCIT_C101662 isDefinedBy ncit.owl @default.
- NCIT_C101662 label "TMEM216 wt Allele" @default.
- NCIT_C101662 subClassOf B31f0c94976063e5c6a7b0f3cb99495f8 @default.
- NCIT_C101662 subClassOf B610d6ef08942cc787315935714ec3326 @default.
- NCIT_C101662 subClassOf NCIT_C101661 @default.
- NCIT_C101662 subClassOf NCIT_C101662 @default.
- NCIT_C101662 subClassOf NCIT_C16612 @default.
- NCIT_C101662 subClassOf NCIT_C20194 @default.
- NCIT_C101662 subClassOf NCIT_C25869 @default.
- NCIT_C101662 subClassOf NCIT_C26039 @default.