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- NCIT_C122662 IAO_0000115 "Glycogen storage disease usually inherited in an X-linked recessive pattern. It is characterized by a deficiency of hepatic phosphorylase kinase." @default.
- NCIT_C122662 NCIT_NHC0 "C122662" @default.
- NCIT_C122662 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C122662 NCIT_P108 "Glycogen Storage Disease Type IX" @default.
- NCIT_C122662 NCIT_P207 "C0268147" @default.
- NCIT_C122662 NCIT_P322 "Cellosaurus" @default.
- NCIT_C122662 normalizedInformationContent "100" @default.
- NCIT_C122662 referenceCount "1" @default.
- NCIT_C122662 hasExactSynonym "Glycogen Storage Disease Type IX" @default.
- NCIT_C122662 hasExactSynonym "Phosphorylase Kinase Deficiency" @default.
- NCIT_C122662 inSubset NCIT_C165258 @default.
- NCIT_C122662 inSubset NCIT_C192842 @default.
- NCIT_C122662 type Class @default.
- NCIT_C122662 isDefinedBy ncit.owl @default.
- NCIT_C122662 label "Glycogen Storage Disease Type IX" @default.
- NCIT_C122662 subClassOf NCIT_C122662 @default.
- NCIT_C122662 subClassOf NCIT_C2991 @default.
- NCIT_C122662 subClassOf NCIT_C3235 @default.
- NCIT_C122662 subClassOf NCIT_C34816 @default.
- NCIT_C122662 subClassOf NCIT_C4873 @default.
- NCIT_C122662 subClassOf NCIT_C53529 @default.
- NCIT_C122662 subClassOf NCIT_C53543 @default.
- NCIT_C122662 subClassOf NCIT_C53547 @default.
- NCIT_C122662 subClassOf NCIT_C61272 @default.
- NCIT_C122662 subClassOf NCIT_C7057 @default.