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Matches in Ubergraph for { <http://purl.obolibrary.org/obo/MONDO_0013027> ?p ?o ?g. }

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MONDO_0013027 RO_0040035 UBERON_0002104 @default.
MONDO_0013027 RO_0040035 UBERON_0003891 @default.
MONDO_0013027 RO_0040035 UBERON_0004088 @default.
MONDO_0013027 RO_0040035 UBERON_0004121 @default.
MONDO_0013027 RO_0040035 UBERON_0004456 @default.
MONDO_0013027 RO_0040035 UBERON_0004923 @default.
MONDO_0013027 RO_0040035 UBERON_0007811 @default.
MONDO_0013027 RO_0040035 UBERON_0010000 @default.
MONDO_0013027 RO_0040035 UBERON_0010230 @default.
MONDO_0013027 RO_0040035 UBERON_0010313 @default.
MONDO_0013027 RO_0040035 UBERON_0010314 @default.
MONDO_0013027 RO_0040035 UBERON_0010409 @default.
MONDO_0013027 RO_0040035 UBERON_0011676 @default.
MONDO_0013027 RO_0040035 UBERON_0012430 @default.
MONDO_0013027 RO_0040035 UBERON_0013701 @default.
MONDO_0013027 RO_0040035 UBERON_0013702 @default.
MONDO_0013027 RO_0040035 UBERON_0015203 @default.
MONDO_0013027 RO_0040035 UBERON_0015212 @default.
MONDO_0013027 RO_0040035 UBERON_0034923 @default.
MONDO_0013027 normalizedInformationContent "100" @default.
MONDO_0013027 referenceCount "1" @default.
MONDO_0013027 hasDbXref "DOID:0060452" @default.
MONDO_0013027 hasDbXref "GARD:16880" @default.
MONDO_0013027 hasDbXref "MESH:C567546" @default.
MONDO_0013027 hasDbXref "OMIM:612868" @default.
MONDO_0013027 hasDbXref "Orphanet:98971" @default.
MONDO_0013027 hasDbXref "SCTID:719296002" @default.
MONDO_0013027 hasDbXref "UMLS:C2748502" @default.
MONDO_0013027 hasExactSynonym "PACD" @default.
MONDO_0013027 hasExactSynonym "posterior amorphous corneal dystrophy" @default.
MONDO_0013027 hasExactSynonym "posterior amorphous stromal dystrophy" @default.
MONDO_0013027 hasRelatedSynonym "chromosome 12Q21.33 deletion syndrome" @default.
MONDO_0013027 hasRelatedSynonym "corneal dystrophy, POSTERIOR amorphous" @default.
MONDO_0013027 id "MONDO:0013027" @default.
MONDO_0013027 inSubset gard_rare @default.
MONDO_0013027 inSubset nord_rare @default.
MONDO_0013027 inSubset ordo_disease @default.
MONDO_0013027 inSubset orphanet_rare @default.
MONDO_0013027 inSubset rare @default.
MONDO_0013027 type Class @default.
MONDO_0013027 isDefinedBy mondo.owl @default.
MONDO_0013027 label "posterior amorphous corneal dystrophy" @default.
MONDO_0013027 subClassOf BFO_0000001 @default.
MONDO_0013027 subClassOf BFO_0000002 @default.
MONDO_0013027 subClassOf BFO_0000016 @default.
MONDO_0013027 subClassOf BFO_0000017 @default.
MONDO_0013027 subClassOf BFO_0000020 @default.
MONDO_0013027 subClassOf COB_0000033 @default.
MONDO_0013027 subClassOf COB_0000111 @default.
MONDO_0013027 subClassOf COB_0000502 @default.
MONDO_0013027 subClassOf MONDO_0000001 @default.
MONDO_0013027 subClassOf MONDO_0000942 @default.
MONDO_0013027 subClassOf MONDO_0002022 @default.
MONDO_0013027 subClassOf MONDO_0005328 @default.
MONDO_0013027 subClassOf MONDO_0013027 @default.
MONDO_0013027 subClassOf MONDO_0018102 @default.
MONDO_0013027 subClassOf MONDO_0020213 @default.
MONDO_0013027 subClassOf MONDO_0024458 @default.
MONDO_0013027 subClassOf MONDO_0700096 @default.
MONDO_0013027 subClassOf OGMS_0000031 @default.
MONDO_0013027 subClassOf PATO_0000001 @default.
MONDO_0013027 exactMatch C567546 @default.
MONDO_0013027 exactMatch 719296002 @default.
MONDO_0013027 exactMatch C2748502 @default.
MONDO_0013027 exactMatch DOID_0060452 @default.
MONDO_0013027 exactMatch Orphanet_98971 @default.
MONDO_0013027 exactMatch 612868 @default.
MONDO_0013027 category Attribute @default.
MONDO_0013027 category BiologicalEntity @default.
MONDO_0013027 category Disease @default.
MONDO_0013027 category DiseaseOrPhenotypicFeature @default.
MONDO_0013027 category Entity @default.
MONDO_0013027 category NamedThing @default.
MONDO_0013027 category OntologyClass @default.
MONDO_0013027 category OrganismAttribute @default.
MONDO_0013027 category PhenotypicQuality @default.
MONDO_0013027 category ThingWithTaxon @default.

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