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- NCIT_C97096 IAO_0000115 "A group of genetic or acquired metabolic disorders characterized by defects in the enzymes that are involved in the heme synthesis." @default.
- NCIT_C97096 NCIT_NHC0 "C97096" @default.
- NCIT_C97096 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C97096 NCIT_P108 "Porphyria" @default.
- NCIT_C97096 NCIT_P207 "C0032708" @default.
- NCIT_C97096 normalizedInformationContent "82.536929774922015" @default.
- NCIT_C97096 referenceCount "14" @default.
- NCIT_C97096 hasExactSynonym "Porphyria" @default.
- NCIT_C97096 type Class @default.
- NCIT_C97096 isDefinedBy ncit.owl @default.
- NCIT_C97096 label "Porphyria" @default.
- NCIT_C97096 subClassOf NCIT_C2991 @default.
- NCIT_C97096 subClassOf NCIT_C3235 @default.
- NCIT_C97096 subClassOf NCIT_C53529 @default.
- NCIT_C97096 subClassOf NCIT_C53547 @default.
- NCIT_C97096 subClassOf NCIT_C7057 @default.
- NCIT_C97096 subClassOf NCIT_C97096 @default.