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- NCIT_C155762 IAO_0000115 "An autosomal recessive condition caused by mutation(s) in the PEX16 gene, encoding peroxisomal membrane protein PEX16. Peroxisome biogenesis disorder 8A manifests phenotypically as Zellweger syndrome." @default.
- NCIT_C155762 NCIT_NHC0 "C155762" @default.
- NCIT_C155762 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C155762 NCIT_P108 "Peroxisome Biogenesis Disorder 8A" @default.
- NCIT_C155762 NCIT_P208 "CL556241" @default.
- NCIT_C155762 NCIT_P322 "Cellosaurus" @default.
- NCIT_C155762 NCIT_R100 NCIT_C12219 @default.
- NCIT_C155762 NCIT_R100 NCIT_C12755 @default.
- NCIT_C155762 NCIT_R100 NCIT_C12919 @default.
- NCIT_C155762 normalizedInformationContent "100" @default.
- NCIT_C155762 referenceCount "1" @default.
- NCIT_C155762 hasExactSynonym "PBD8A" @default.
- NCIT_C155762 hasExactSynonym "Peroxisome Biogenesis Disorder 8A" @default.
- NCIT_C155762 inSubset NCIT_C165258 @default.
- NCIT_C155762 inSubset NCIT_C192842 @default.
- NCIT_C155762 type Class @default.
- NCIT_C155762 isDefinedBy ncit.owl @default.
- NCIT_C155762 label "Peroxisome Biogenesis Disorder 8A" @default.
- NCIT_C155762 subClassOf NCIT_C155747 @default.
- NCIT_C155762 subClassOf NCIT_C155762 @default.
- NCIT_C155762 subClassOf NCIT_C26835 @default.
- NCIT_C155762 subClassOf NCIT_C27551 @default.
- NCIT_C155762 subClassOf NCIT_C27588 @default.
- NCIT_C155762 subClassOf NCIT_C2991 @default.
- NCIT_C155762 subClassOf NCIT_C4873 @default.
- NCIT_C155762 subClassOf NCIT_C53529 @default.
- NCIT_C155762 subClassOf NCIT_C53531 @default.
- NCIT_C155762 subClassOf NCIT_C53543 @default.
- NCIT_C155762 subClassOf NCIT_C53547 @default.
- NCIT_C155762 subClassOf NCIT_C61253 @default.
- NCIT_C155762 subClassOf NCIT_C7057 @default.