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- NCIT_C186307 IAO_0000115 "A genetic condition, caused by mutation(s) in the DDX24 gene, encoding ATP-dependent RNA helicase DDX24. It is associated with vascular stenosis of portal and hepatic veins and/or lymphatic vessels." @default.
- NCIT_C186307 NCIT_NHC0 "C186307" @default.
- NCIT_C186307 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C186307 NCIT_P108 "Multiorgan Venous and Lymphatic Defect Syndrome" @default.
- NCIT_C186307 NCIT_P208 "CL1778651" @default.
- NCIT_C186307 NCIT_P322 "Cellosaurus" @default.
- NCIT_C186307 NCIT_R176 NCIT_C16612 @default.
- NCIT_C186307 NCIT_R176 NCIT_C200772 @default.
- NCIT_C186307 NCIT_R176 NCIT_C21281 @default.
- NCIT_C186307 NCIT_R176 NCIT_C25804 @default.
- NCIT_C186307 NCIT_R176 NCIT_C26057 @default.
- NCIT_C186307 normalizedInformationContent "100" @default.
- NCIT_C186307 referenceCount "1" @default.
- NCIT_C186307 hasExactSynonym "MOVLD" @default.
- NCIT_C186307 hasExactSynonym "Multiorgan Venous and Lymphatic Defect Syndrome" @default.
- NCIT_C186307 inSubset NCIT_C165258 @default.
- NCIT_C186307 inSubset NCIT_C192842 @default.
- NCIT_C186307 type Class @default.
- NCIT_C186307 isDefinedBy ncit.owl @default.
- NCIT_C186307 label "Multiorgan Venous and Lymphatic Defect Syndrome" @default.
- NCIT_C186307 subClassOf B7d52a8100b3b5a2882e038846fb65880 @default.
- NCIT_C186307 subClassOf Bc67beb4a371d99317ed077713a1881ae @default.
- NCIT_C186307 subClassOf NCIT_C186307 @default.
- NCIT_C186307 subClassOf NCIT_C28193 @default.
- NCIT_C186307 subClassOf NCIT_C2991 @default.
- NCIT_C186307 subClassOf NCIT_C7057 @default.