Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C84705> ?p ?o ?g. }
Showing items 1 to 50 of
50
with 100 items per page.
- NCIT_C84705 IAO_0000115 "A rare inherited bleeding disorder caused by deficiency of coagulation factor XI. It may be asymptomatic or manifest with bleeding." @default.
- NCIT_C84705 NCIT_NHC0 "C84705" @default.
- NCIT_C84705 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C84705 NCIT_P108 "Hereditary Factor XI Deficiency" @default.
- NCIT_C84705 NCIT_P207 "C0015523" @default.
- NCIT_C84705 NCIT_P322 "NICHD" @default.
- NCIT_C84705 NCIT_P322 "mCode" @default.
- NCIT_C84705 NCIT_P325 "An autosomal recessive, inherited coagulation disorder characterized by the partial or complete absence of factor XI activity in the blood." @default.
- NCIT_C84705 NCIT_R100 NCIT_C12219 @default.
- NCIT_C84705 NCIT_R100 NCIT_C12919 @default.
- NCIT_C84705 NCIT_R100 NCIT_C41165 @default.
- NCIT_C84705 NCIT_R101 NCIT_C12219 @default.
- NCIT_C84705 NCIT_R101 NCIT_C12919 @default.
- NCIT_C84705 NCIT_R101 NCIT_C41165 @default.
- NCIT_C84705 NCIT_R103 NCIT_C12219 @default.
- NCIT_C84705 NCIT_R103 NCIT_C12801 @default.
- NCIT_C84705 NCIT_R103 NCIT_C41168 @default.
- NCIT_C84705 NCIT_R104 NCIT_C12219 @default.
- NCIT_C84705 NCIT_R104 NCIT_C12508 @default.
- NCIT_C84705 NCIT_R104 NCIT_C21599 @default.
- NCIT_C84705 NCIT_R104 NCIT_C32725 @default.
- NCIT_C84705 normalizedInformationContent "100" @default.
- NCIT_C84705 referenceCount "1" @default.
- NCIT_C84705 hasExactSynonym "Hemophilia C" @default.
- NCIT_C84705 hasExactSynonym "Hereditary Factor XI Deficiency Disease" @default.
- NCIT_C84705 hasExactSynonym "Hereditary Factor XI Deficiency" @default.
- NCIT_C84705 hasExactSynonym "Hereditary factor XI deficiency" @default.
- NCIT_C84705 inSubset NCIT_C132009 @default.
- NCIT_C84705 inSubset NCIT_C193006 @default.
- NCIT_C84705 inSubset NCIT_C193181 @default.
- NCIT_C84705 inSubset NCIT_C90259 @default.
- NCIT_C84705 inSubset NCIT_C99147 @default.
- NCIT_C84705 type Class @default.
- NCIT_C84705 isDefinedBy ncit.owl @default.
- NCIT_C84705 label "Hereditary Factor XI Deficiency" @default.
- NCIT_C84705 subClassOf NCIT_C104003 @default.
- NCIT_C84705 subClassOf NCIT_C131739 @default.
- NCIT_C84705 subClassOf NCIT_C26323 @default.
- NCIT_C84705 subClassOf NCIT_C26324 @default.
- NCIT_C84705 subClassOf NCIT_C27215 @default.
- NCIT_C84705 subClassOf NCIT_C27551 @default.
- NCIT_C84705 subClassOf NCIT_C2902 @default.
- NCIT_C84705 subClassOf NCIT_C2991 @default.
- NCIT_C84705 subClassOf NCIT_C3093 @default.
- NCIT_C84705 subClassOf NCIT_C35814 @default.
- NCIT_C84705 subClassOf NCIT_C53529 @default.
- NCIT_C84705 subClassOf NCIT_C53531 @default.
- NCIT_C84705 subClassOf NCIT_C7057 @default.
- NCIT_C84705 subClassOf NCIT_C84705 @default.
- NCIT_C84705 subClassOf NCIT_C98942 @default.