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- NCIT_C85002 IAO_0000115 "An autosomal dominant inherited condition caused by mutations in the lamin B receptor gene. It is characterized by defects in the neutrophil lobulation, resulting in the presence of dumbbell-shaped neutrophils with bilobed nuclei in the peripheral blood smear." @default.
- NCIT_C85002 NCIT_NHC0 "C85002" @default.
- NCIT_C85002 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C85002 NCIT_P108 "Pelger-Huet Anomaly" @default.
- NCIT_C85002 NCIT_P207 "C0030779" @default.
- NCIT_C85002 NCIT_R100 NCIT_C12219 @default.
- NCIT_C85002 NCIT_R100 NCIT_C12919 @default.
- NCIT_C85002 NCIT_R100 NCIT_C41165 @default.
- NCIT_C85002 NCIT_R101 NCIT_C12219 @default.
- NCIT_C85002 NCIT_R101 NCIT_C12919 @default.
- NCIT_C85002 NCIT_R101 NCIT_C41165 @default.
- NCIT_C85002 NCIT_R103 NCIT_C12219 @default.
- NCIT_C85002 NCIT_R103 NCIT_C12801 @default.
- NCIT_C85002 NCIT_R103 NCIT_C41168 @default.
- NCIT_C85002 NCIT_R104 NCIT_C12219 @default.
- NCIT_C85002 NCIT_R104 NCIT_C12508 @default.
- NCIT_C85002 NCIT_R104 NCIT_C21599 @default.
- NCIT_C85002 NCIT_R104 NCIT_C32725 @default.
- NCIT_C85002 normalizedInformationContent "100" @default.
- NCIT_C85002 referenceCount "1" @default.
- NCIT_C85002 hasExactSynonym "Pelger-Huet Anomaly" @default.
- NCIT_C85002 type Class @default.
- NCIT_C85002 isDefinedBy ncit.owl @default.
- NCIT_C85002 label "Pelger-Huet Anomaly" @default.
- NCIT_C85002 subClassOf NCIT_C171089 @default.
- NCIT_C85002 subClassOf NCIT_C26323 @default.
- NCIT_C85002 subClassOf NCIT_C26324 @default.
- NCIT_C85002 subClassOf NCIT_C27551 @default.
- NCIT_C85002 subClassOf NCIT_C2991 @default.
- NCIT_C85002 subClassOf NCIT_C35814 @default.
- NCIT_C85002 subClassOf NCIT_C4873 @default.
- NCIT_C85002 subClassOf NCIT_C53529 @default.
- NCIT_C85002 subClassOf NCIT_C53531 @default.
- NCIT_C85002 subClassOf NCIT_C53543 @default.
- NCIT_C85002 subClassOf NCIT_C53547 @default.
- NCIT_C85002 subClassOf NCIT_C7057 @default.
- NCIT_C85002 subClassOf NCIT_C85002 @default.