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- NCIT_C26799 IAO_0000115 "A very rare autosomal recessive inherited blood coagulation disorder characterized by deficiency of prothrombin, resulting in bleeding." @default.
- NCIT_C26799 NCIT_NHC0 "C26799" @default.
- NCIT_C26799 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C26799 NCIT_P108 "Hereditary Factor II Deficiency" @default.
- NCIT_C26799 NCIT_P207 "C0272317" @default.
- NCIT_C26799 NCIT_P322 "Cellosaurus" @default.
- NCIT_C26799 NCIT_P322 "NICHD" @default.
- NCIT_C26799 NCIT_P325 "An autosomal recessive, inherited coagulation disorder characterized by the partial or complete absence of prothrombin (factor II) activity in the blood." @default.
- NCIT_C26799 NCIT_P366 "Factor_II_Deficiency" @default.
- NCIT_C26799 NCIT_R100 NCIT_C12219 @default.
- NCIT_C26799 NCIT_R100 NCIT_C12919 @default.
- NCIT_C26799 NCIT_R100 NCIT_C41165 @default.
- NCIT_C26799 NCIT_R101 NCIT_C12219 @default.
- NCIT_C26799 NCIT_R101 NCIT_C12919 @default.
- NCIT_C26799 NCIT_R101 NCIT_C41165 @default.
- NCIT_C26799 NCIT_R103 NCIT_C12219 @default.
- NCIT_C26799 NCIT_R103 NCIT_C12801 @default.
- NCIT_C26799 NCIT_R103 NCIT_C41168 @default.
- NCIT_C26799 NCIT_R104 NCIT_C12219 @default.
- NCIT_C26799 NCIT_R104 NCIT_C12508 @default.
- NCIT_C26799 NCIT_R104 NCIT_C21599 @default.
- NCIT_C26799 NCIT_R104 NCIT_C32725 @default.
- NCIT_C26799 NCIT_R176 NCIT_C16612 @default.
- NCIT_C26799 NCIT_R176 NCIT_C21281 @default.
- NCIT_C26799 NCIT_R176 NCIT_C21295 @default.
- NCIT_C26799 NCIT_R176 NCIT_C25804 @default.
- NCIT_C26799 NCIT_R176 NCIT_C26003 @default.
- NCIT_C26799 NCIT_R176 NCIT_C28480 @default.
- NCIT_C26799 NCIT_R176 NCIT_C82852 @default.
- NCIT_C26799 normalizedInformationContent "100" @default.
- NCIT_C26799 referenceCount "1" @default.
- NCIT_C26799 hasExactSynonym "Hereditary Factor II Deficiency" @default.
- NCIT_C26799 hasExactSynonym "Hereditary Hypoprothrombinemia" @default.
- NCIT_C26799 hasExactSynonym "Hereditary Prothrombin Deficiency" @default.
- NCIT_C26799 inSubset NCIT_C132009 @default.
- NCIT_C26799 inSubset NCIT_C165258 @default.
- NCIT_C26799 inSubset NCIT_C192842 @default.
- NCIT_C26799 inSubset NCIT_C90259 @default.
- NCIT_C26799 inSubset NCIT_C99147 @default.
- NCIT_C26799 type Class @default.
- NCIT_C26799 isDefinedBy ncit.owl @default.
- NCIT_C26799 label "Hereditary Factor II Deficiency" @default.
- NCIT_C26799 subClassOf B3177662a9a7094cc12eb0c52d9511bd3 @default.
- NCIT_C26799 subClassOf B64a9bab5c725865a08ae67f19784d83c @default.
- NCIT_C26799 subClassOf NCIT_C104003 @default.
- NCIT_C26799 subClassOf NCIT_C131737 @default.
- NCIT_C26799 subClassOf NCIT_C26323 @default.
- NCIT_C26799 subClassOf NCIT_C26324 @default.
- NCIT_C26799 subClassOf NCIT_C26799 @default.
- NCIT_C26799 subClassOf NCIT_C27215 @default.
- NCIT_C26799 subClassOf NCIT_C27551 @default.
- NCIT_C26799 subClassOf NCIT_C2902 @default.
- NCIT_C26799 subClassOf NCIT_C2991 @default.
- NCIT_C26799 subClassOf NCIT_C35814 @default.
- NCIT_C26799 subClassOf NCIT_C53529 @default.
- NCIT_C26799 subClassOf NCIT_C53531 @default.
- NCIT_C26799 subClassOf NCIT_C7057 @default.
- NCIT_C26799 subClassOf NCIT_C98942 @default.