Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C26721> ?p ?o ?g. }
Showing items 1 to 64 of
64
with 100 items per page.
- NCIT_C26721 IAO_0000115 "An X-linked inherited bleeding disorder caused by deficiency of the coagulation factor IX." @default.
- NCIT_C26721 NCIT_NHC0 "C26721" @default.
- NCIT_C26721 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C26721 NCIT_P108 "Hemophilia B" @default.
- NCIT_C26721 NCIT_P207 "C0008533" @default.
- NCIT_C26721 NCIT_P322 "Cellosaurus" @default.
- NCIT_C26721 NCIT_P322 "NICHD" @default.
- NCIT_C26721 NCIT_P322 "mCode" @default.
- NCIT_C26721 NCIT_P325 "An X-linked recessive deficiency of coagulation factor IX characterized by a tendency to bleed. Hemophilia B occurs in approximately 1 in 20,000 live male births." @default.
- NCIT_C26721 NCIT_P366 "Hemophilia_B" @default.
- NCIT_C26721 NCIT_R100 NCIT_C12219 @default.
- NCIT_C26721 NCIT_R100 NCIT_C12919 @default.
- NCIT_C26721 NCIT_R100 NCIT_C41165 @default.
- NCIT_C26721 NCIT_R101 NCIT_C12219 @default.
- NCIT_C26721 NCIT_R101 NCIT_C12919 @default.
- NCIT_C26721 NCIT_R101 NCIT_C41165 @default.
- NCIT_C26721 NCIT_R103 NCIT_C12219 @default.
- NCIT_C26721 NCIT_R103 NCIT_C12801 @default.
- NCIT_C26721 NCIT_R103 NCIT_C41168 @default.
- NCIT_C26721 NCIT_R104 NCIT_C12219 @default.
- NCIT_C26721 NCIT_R104 NCIT_C12508 @default.
- NCIT_C26721 NCIT_R104 NCIT_C21599 @default.
- NCIT_C26721 NCIT_R104 NCIT_C32725 @default.
- NCIT_C26721 NCIT_R176 NCIT_C16612 @default.
- NCIT_C26721 NCIT_R176 NCIT_C21281 @default.
- NCIT_C26721 NCIT_R176 NCIT_C21295 @default.
- NCIT_C26721 NCIT_R176 NCIT_C25804 @default.
- NCIT_C26721 NCIT_R176 NCIT_C26003 @default.
- NCIT_C26721 NCIT_R176 NCIT_C28480 @default.
- NCIT_C26721 NCIT_R176 NCIT_C28481 @default.
- NCIT_C26721 normalizedInformationContent "90.826665450122817" @default.
- NCIT_C26721 referenceCount "4" @default.
- NCIT_C26721 hasExactSynonym "Christmas Disease" @default.
- NCIT_C26721 hasExactSynonym "Factor IX Deficiency" @default.
- NCIT_C26721 hasExactSynonym "Hemophilia B" @default.
- NCIT_C26721 hasExactSynonym "Hereditary Factor IX Deficiency Disease" @default.
- NCIT_C26721 hasExactSynonym "Hereditary Factor IX Deficiency" @default.
- NCIT_C26721 hasExactSynonym "Hereditary factor IX deficiency" @default.
- NCIT_C26721 inSubset NCIT_C132009 @default.
- NCIT_C26721 inSubset NCIT_C165258 @default.
- NCIT_C26721 inSubset NCIT_C192842 @default.
- NCIT_C26721 inSubset NCIT_C193006 @default.
- NCIT_C26721 inSubset NCIT_C193181 @default.
- NCIT_C26721 inSubset NCIT_C90259 @default.
- NCIT_C26721 inSubset NCIT_C99147 @default.
- NCIT_C26721 type Class @default.
- NCIT_C26721 isDefinedBy ncit.owl @default.
- NCIT_C26721 label "Hemophilia B" @default.
- NCIT_C26721 subClassOf B2587c5beb1f6d7eafe54e0c5ec031011 @default.
- NCIT_C26721 subClassOf Bb77a4b2fbd327ae0a7b20ef24993b909 @default.
- NCIT_C26721 subClassOf NCIT_C104003 @default.
- NCIT_C26721 subClassOf NCIT_C26323 @default.
- NCIT_C26721 subClassOf NCIT_C26324 @default.
- NCIT_C26721 subClassOf NCIT_C26721 @default.
- NCIT_C26721 subClassOf NCIT_C27215 @default.
- NCIT_C26721 subClassOf NCIT_C27551 @default.
- NCIT_C26721 subClassOf NCIT_C2902 @default.
- NCIT_C26721 subClassOf NCIT_C2991 @default.
- NCIT_C26721 subClassOf NCIT_C3093 @default.
- NCIT_C26721 subClassOf NCIT_C35814 @default.
- NCIT_C26721 subClassOf NCIT_C53529 @default.
- NCIT_C26721 subClassOf NCIT_C53531 @default.
- NCIT_C26721 subClassOf NCIT_C7057 @default.
- NCIT_C26721 subClassOf NCIT_C98942 @default.