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- NCIT_C26770 IAO_0000115 "A rare autosomal recessive inherited bleeding disorder caused by deficiency of coagulation factor XII. It may be asymptomatic or manifest with bleeding." @default.
- NCIT_C26770 NCIT_NHC0 "C26770" @default.
- NCIT_C26770 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C26770 NCIT_P108 "Hereditary Factor XII Deficiency" @default.
- NCIT_C26770 NCIT_P207 "C0272334" @default.
- NCIT_C26770 NCIT_P322 "NICHD" @default.
- NCIT_C26770 NCIT_P325 "An autosomal recessive, inherited coagulation disorder characterized by the partial or complete absence of factor XII activity in the blood." @default.
- NCIT_C26770 NCIT_P366 "Factor_XII_Deficiency" @default.
- NCIT_C26770 NCIT_R100 NCIT_C12219 @default.
- NCIT_C26770 NCIT_R100 NCIT_C12919 @default.
- NCIT_C26770 NCIT_R100 NCIT_C41165 @default.
- NCIT_C26770 NCIT_R101 NCIT_C12219 @default.
- NCIT_C26770 NCIT_R101 NCIT_C12919 @default.
- NCIT_C26770 NCIT_R101 NCIT_C41165 @default.
- NCIT_C26770 NCIT_R103 NCIT_C12219 @default.
- NCIT_C26770 NCIT_R103 NCIT_C12801 @default.
- NCIT_C26770 NCIT_R103 NCIT_C41168 @default.
- NCIT_C26770 NCIT_R104 NCIT_C12219 @default.
- NCIT_C26770 NCIT_R104 NCIT_C12508 @default.
- NCIT_C26770 NCIT_R104 NCIT_C21599 @default.
- NCIT_C26770 NCIT_R104 NCIT_C32725 @default.
- NCIT_C26770 NCIT_R176 NCIT_C104215 @default.
- NCIT_C26770 NCIT_R176 NCIT_C16612 @default.
- NCIT_C26770 NCIT_R176 NCIT_C21281 @default.
- NCIT_C26770 NCIT_R176 NCIT_C21295 @default.
- NCIT_C26770 NCIT_R176 NCIT_C25804 @default.
- NCIT_C26770 NCIT_R176 NCIT_C26003 @default.
- NCIT_C26770 NCIT_R176 NCIT_C28480 @default.
- NCIT_C26770 normalizedInformationContent "100" @default.
- NCIT_C26770 referenceCount "1" @default.
- NCIT_C26770 hasExactSynonym "Hereditary Factor XII Deficiency Disease" @default.
- NCIT_C26770 hasExactSynonym "Hereditary Factor XII Deficiency" @default.
- NCIT_C26770 hasExactSynonym "Hereditary Hageman Factor Deficiency" @default.
- NCIT_C26770 inSubset NCIT_C132009 @default.
- NCIT_C26770 inSubset NCIT_C90259 @default.
- NCIT_C26770 inSubset NCIT_C99147 @default.
- NCIT_C26770 type Class @default.
- NCIT_C26770 isDefinedBy ncit.owl @default.
- NCIT_C26770 label "Hereditary Factor XII Deficiency" @default.
- NCIT_C26770 subClassOf B415ba3bc051d4a48d6589aa0bdd0b576 @default.
- NCIT_C26770 subClassOf B571d93ca8fa63aebb311bb061737a749 @default.
- NCIT_C26770 subClassOf NCIT_C104003 @default.
- NCIT_C26770 subClassOf NCIT_C131740 @default.
- NCIT_C26770 subClassOf NCIT_C26323 @default.
- NCIT_C26770 subClassOf NCIT_C26324 @default.
- NCIT_C26770 subClassOf NCIT_C26770 @default.
- NCIT_C26770 subClassOf NCIT_C27215 @default.
- NCIT_C26770 subClassOf NCIT_C27551 @default.
- NCIT_C26770 subClassOf NCIT_C2902 @default.
- NCIT_C26770 subClassOf NCIT_C2991 @default.
- NCIT_C26770 subClassOf NCIT_C35814 @default.
- NCIT_C26770 subClassOf NCIT_C53529 @default.
- NCIT_C26770 subClassOf NCIT_C53531 @default.
- NCIT_C26770 subClassOf NCIT_C7057 @default.
- NCIT_C26770 subClassOf NCIT_C98942 @default.