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- NCIT_C185732 IAO_0000115 "Human ARHGAP31 wild-type allele is located within 3q13.32-q13.33 and is approximately 126 kb in length. This allele, which encodes Rho GTPase-activating protein 31, is involved in the regulation of GTPase activities of RAC1 and CDC42. Mutation of the gene is associated with Adams-Oliver syndrome 1." @default.
- NCIT_C185732 NCIT_NHC0 "C185732" @default.
- NCIT_C185732 NCIT_P100 "610911" @default.
- NCIT_C185732 NCIT_P102 "NM_020754" @default.
- NCIT_C185732 NCIT_P106 "Gene or Genome" @default.
- NCIT_C185732 NCIT_P108 "ARHGAP31 wt Allele" @default.
- NCIT_C185732 NCIT_P208 "CL1778346" @default.
- NCIT_C185732 NCIT_P321 "57514" @default.
- NCIT_C185732 NCIT_R37 NCIT_C17133 @default.
- NCIT_C185732 NCIT_R37 NCIT_C17828 @default.
- NCIT_C185732 NCIT_R37 NCIT_C20480 @default.
- NCIT_C185732 NCIT_R41 NCIT_C14182 @default.
- NCIT_C185732 NCIT_R41 NCIT_C14225 @default.
- NCIT_C185732 NCIT_R41 NCIT_C14234 @default.
- NCIT_C185732 NCIT_R41 NCIT_C14250 @default.
- NCIT_C185732 NCIT_R41 NCIT_C14262 @default.
- NCIT_C185732 NCIT_R41 NCIT_C14282 @default.
- NCIT_C185732 NCIT_R41 NCIT_C25796 @default.
- NCIT_C185732 NCIT_R41 NCIT_C79740 @default.
- NCIT_C185732 normalizedInformationContent "100" @default.
- NCIT_C185732 referenceCount "1" @default.
- NCIT_C185732 hasExactSynonym "AOS1" @default.
- NCIT_C185732 hasExactSynonym "ARHGAP31 wt Allele" @default.
- NCIT_C185732 hasExactSynonym "CDGAP" @default.
- NCIT_C185732 hasExactSynonym "KIAA1204" @default.
- NCIT_C185732 hasExactSynonym "Rho GTPase Activating Protein 31 wt Allele" @default.
- NCIT_C185732 type Class @default.
- NCIT_C185732 isDefinedBy ncit.owl @default.
- NCIT_C185732 label "ARHGAP31 wt Allele" @default.
- NCIT_C185732 subClassOf NCIT_C16612 @default.
- NCIT_C185732 subClassOf NCIT_C185731 @default.
- NCIT_C185732 subClassOf NCIT_C185732 @default.
- NCIT_C185732 subClassOf NCIT_C20921 @default.