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- NCIT_C118546 IAO_0000115 "Human ABHD12 wild-type allele is located in the vicinity of 20p11.21 and is approximately 96 kb in length. This allele, which encodes monoacylglycerol lipase ABHD12 protein, is involved in endocannabinoid catabolism. Mutation of the gene is associated with the neurological disorder, polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract." @default.
- NCIT_C118546 NCIT_NHC0 "C118546" @default.
- NCIT_C118546 NCIT_P100 "613599" @default.
- NCIT_C118546 NCIT_P102 "AL117442" @default.
- NCIT_C118546 NCIT_P106 "Gene or Genome" @default.
- NCIT_C118546 NCIT_P107 "ABHD12 wt Allele" @default.
- NCIT_C118546 NCIT_P108 "ABHD12 wt Allele" @default.
- NCIT_C118546 NCIT_P207 "C3890226" @default.
- NCIT_C118546 NCIT_P321 "26090" @default.
- NCIT_C118546 NCIT_P322 "CTRP" @default.
- NCIT_C118546 NCIT_R37 NCIT_C16702 @default.
- NCIT_C118546 NCIT_R37 NCIT_C16841 @default.
- NCIT_C118546 NCIT_R37 NCIT_C17710 @default.
- NCIT_C118546 NCIT_R37 NCIT_C17828 @default.
- NCIT_C118546 NCIT_R37 NCIT_C19405 @default.
- NCIT_C118546 NCIT_R37 NCIT_C19536 @default.
- NCIT_C118546 NCIT_R37 NCIT_C19899 @default.
- NCIT_C118546 NCIT_R37 NCIT_C21198 @default.
- NCIT_C118546 NCIT_R37 NCIT_C28498 @default.
- NCIT_C118546 NCIT_R37 NCIT_C41578 @default.
- NCIT_C118546 NCIT_R41 NCIT_C14182 @default.
- NCIT_C118546 NCIT_R41 NCIT_C14225 @default.
- NCIT_C118546 NCIT_R41 NCIT_C14234 @default.
- NCIT_C118546 NCIT_R41 NCIT_C14250 @default.
- NCIT_C118546 NCIT_R41 NCIT_C14262 @default.
- NCIT_C118546 NCIT_R41 NCIT_C14282 @default.
- NCIT_C118546 NCIT_R41 NCIT_C25796 @default.
- NCIT_C118546 NCIT_R41 NCIT_C79740 @default.
- NCIT_C118546 normalizedInformationContent "100" @default.
- NCIT_C118546 referenceCount "1" @default.
- NCIT_C118546 hasExactSynonym "ABHD12 wt Allele" @default.
- NCIT_C118546 hasExactSynonym "ABHD12A" @default.
- NCIT_C118546 hasExactSynonym "Abhydrolase Domain Containing 12 wt Allele" @default.
- NCIT_C118546 hasExactSynonym "BEM46L2" @default.
- NCIT_C118546 hasExactSynonym "C20orf22" @default.
- NCIT_C118546 hasExactSynonym "Chromosome 20 Open Reading Frame 22 Gene" @default.
- NCIT_C118546 hasExactSynonym "DKFZP434P106" @default.
- NCIT_C118546 hasExactSynonym "PHARC" @default.
- NCIT_C118546 hasExactSynonym "RP5-965G21.2" @default.
- NCIT_C118546 hasExactSynonym "dJ965G21.2" @default.
- NCIT_C118546 inSubset NCIT_C116977 @default.
- NCIT_C118546 inSubset NCIT_C142799 @default.
- NCIT_C118546 inSubset NCIT_C142800 @default.
- NCIT_C118546 type Class @default.
- NCIT_C118546 isDefinedBy ncit.owl @default.
- NCIT_C118546 label "ABHD12 wt Allele" @default.
- NCIT_C118546 subClassOf NCIT_C118545 @default.
- NCIT_C118546 subClassOf NCIT_C118546 @default.
- NCIT_C118546 subClassOf NCIT_C16612 @default.
- NCIT_C118546 subClassOf NCIT_C21281 @default.
- NCIT_C118546 subClassOf NCIT_C25804 @default.
- NCIT_C118546 subClassOf NCIT_C25952 @default.