Matches in Ubergraph for { <http://purl.obolibrary.org/obo/HP_0008186> ?p ?o ?g. }
- HP_0008186 UPHENO_0000001 UBERON_0004121 @default.
- HP_0008186 UPHENO_0000001 UBERON_0005172 @default.
- HP_0008186 UPHENO_0000001 UBERON_0005173 @default.
- HP_0008186 UPHENO_0000001 UBERON_0005177 @default.
- HP_0008186 UPHENO_0000001 UBERON_0006858 @default.
- HP_0008186 UPHENO_0000001 UBERON_0009569 @default.
- HP_0008186 UPHENO_0000001 UBERON_0010000 @default.
- HP_0008186 UPHENO_0000001 UBERON_0010074 @default.
- HP_0008186 UPHENO_0000001 UBERON_0010313 @default.
- HP_0008186 UPHENO_0000001 UBERON_0010314 @default.
- HP_0008186 UPHENO_0000001 UBERON_0011216 @default.
- HP_0008186 UPHENO_0000001 UBERON_0011676 @default.
- HP_0008186 UPHENO_0000001 UBERON_0013701 @default.
- HP_0008186 UPHENO_0000001 UBERON_0013702 @default.
- HP_0008186 UPHENO_0000001 UBERON_0015203 @default.
- HP_0008186 UPHENO_0000001 UBERON_0015204 @default.
- HP_0008186 UPHENO_0000001 UBERON_0015212 @default.
- HP_0008186 UPHENO_0000001 UBERON_0034923 @default.
- HP_0008186 normalizedInformationContent "100" @default.
- HP_0008186 referenceCount "1" @default.
- HP_0008186 hasDbXref "UMLS:C1851720" @default.
- HP_0008186 id "HP:0008186" @default.
- HP_0008186 type Class @default.
- HP_0008186 comment "This feature is common in Beckwith Wiedemann syndrome." @default.
- HP_0008186 isDefinedBy hp.owl @default.
- HP_0008186 label "Adrenocortical cytomegaly" @default.
- HP_0008186 subClassOf BFO_0000001 @default.
- HP_0008186 subClassOf BFO_0000002 @default.
- HP_0008186 subClassOf BFO_0000020 @default.
- HP_0008186 subClassOf COB_0000502 @default.
- HP_0008186 subClassOf FBcv_0000000 @default.
- HP_0008186 subClassOf FBcv_0000013 @default.
- HP_0008186 subClassOf FBcv_0000347 @default.
- HP_0008186 subClassOf FBcv_0000807 @default.
- HP_0008186 subClassOf FBcv_0001347 @default.
- HP_0008186 subClassOf HP_0000001 @default.
- HP_0008186 subClassOf HP_0000118 @default.
- HP_0008186 subClassOf HP_0000818 @default.
- HP_0008186 subClassOf HP_0000834 @default.
- HP_0008186 subClassOf HP_0008186 @default.
- HP_0008186 subClassOf HP_0011732 @default.
- HP_0008186 subClassOf HP_0031071 @default.
- HP_0008186 subClassOf MP_0000001 @default.
- HP_0008186 subClassOf MP_0000639 @default.
- HP_0008186 subClassOf MP_0002163 @default.
- HP_0008186 subClassOf MP_0005379 @default.
- HP_0008186 subClassOf MP_0013560 @default.
- HP_0008186 subClassOf PATO_0000001 @default.
- HP_0008186 subClassOf UPHENO_0001001 @default.
- HP_0008186 category Attribute @default.
- HP_0008186 category BiologicalEntity @default.
- HP_0008186 category DiseaseOrPhenotypicFeature @default.
- HP_0008186 category Entity @default.
- HP_0008186 category NamedThing @default.
- HP_0008186 category OntologyClass @default.
- HP_0008186 category OrganismAttribute @default.
- HP_0008186 category PathologicalEntityMixin @default.
- HP_0008186 category PhenotypicFeature @default.
- HP_0008186 category PhenotypicQuality @default.
- HP_0008186 category ThingWithTaxon @default.