FRINK Linked Data Fragments server

Matches in Ubergraph for { <http://purl.obolibrary.org/obo/MONDO_0009788> ?p ?o ?g. }

• MONDO_0009788 disease_shares_features_of COB_0000111 @default.
• MONDO_0009788 disease_shares_features_of COB_0000502 @default.
• MONDO_0009788 disease_shares_features_of MONDO_0000001 @default.
• MONDO_0009788 disease_shares_features_of MONDO_0000425 @default.
• MONDO_0009788 disease_shares_features_of MONDO_0003620 @default.
• MONDO_0009788 disease_shares_features_of MONDO_0003847 @default.
• MONDO_0009788 disease_shares_features_of MONDO_0005066 @default.
• MONDO_0009788 disease_shares_features_of MONDO_0005071 @default.
• MONDO_0009788 disease_shares_features_of MONDO_0005244 @default.
• MONDO_0009788 disease_shares_features_of MONDO_0010699 @default.
• MONDO_0009788 disease_shares_features_of MONDO_0015626 @default.
• MONDO_0009788 disease_shares_features_of MONDO_0018994 @default.
• MONDO_0009788 disease_shares_features_of MONDO_0019052 @default.
• MONDO_0009788 disease_shares_features_of MONDO_0019056 @default.
• MONDO_0009788 disease_shares_features_of MONDO_0019236 @default.
• MONDO_0009788 disease_shares_features_of MONDO_0019254 @default.
• MONDO_0009788 disease_shares_features_of MONDO_0020127 @default.
• MONDO_0009788 disease_shares_features_of MONDO_0037829 @default.
• MONDO_0009788 disease_shares_features_of MONDO_0700096 @default.
• MONDO_0009788 disease_shares_features_of OGMS_0000031 @default.
• MONDO_0009788 disease_shares_features_of PATO_0000001 @default.
• MONDO_0009788 normalizedInformationContent "100" @default.
• MONDO_0009788 referenceCount "1" @default.
• MONDO_0009788 hasDbXref "OMIM:258650" @default.
• MONDO_0009788 hasDbXref "UMLS:C1839566" @default.
• MONDO_0009788 hasExactSynonym "optic atrophy, hearing loss, and peripheral neuropathy, autosomal recessive" @default.
• MONDO_0009788 id "MONDO:0009788" @default.
• MONDO_0009788 type Class @default.
• MONDO_0009788 isDefinedBy mondo.owl @default.
• MONDO_0009788 label "optic atrophy, hearing loss, and peripheral neuropathy, autosomal recessive" @default.
• MONDO_0009788 subClassOf B285637e54d01d78e31288d89330336f1 @default.
• MONDO_0009788 subClassOf B5f18987ca62b04d52b43b920a6031961 @default.
• MONDO_0009788 subClassOf BFO_0000001 @default.
• MONDO_0009788 subClassOf BFO_0000002 @default.
• MONDO_0009788 subClassOf BFO_0000016 @default.
• MONDO_0009788 subClassOf BFO_0000017 @default.
• MONDO_0009788 subClassOf BFO_0000020 @default.
• MONDO_0009788 subClassOf COB_0000033 @default.
• MONDO_0009788 subClassOf COB_0000111 @default.
• MONDO_0009788 subClassOf COB_0000502 @default.
• MONDO_0009788 subClassOf MONDO_0000001 @default.
• MONDO_0009788 subClassOf MONDO_0003847 @default.
• MONDO_0009788 subClassOf MONDO_0009788 @default.
• MONDO_0009788 subClassOf MONDO_0700096 @default.
• MONDO_0009788 subClassOf PATO_0000001 @default.
• MONDO_0009788 exactMatch 258650 @default.
• MONDO_0009788 category Attribute @default.
• MONDO_0009788 category BiologicalEntity @default.
• MONDO_0009788 category Disease @default.
• MONDO_0009788 category DiseaseOrPhenotypicFeature @default.
• MONDO_0009788 category Entity @default.
• MONDO_0009788 category NamedThing @default.
• MONDO_0009788 category OntologyClass @default.
• MONDO_0009788 category OrganismAttribute @default.
• MONDO_0009788 category PhenotypicQuality @default.
• MONDO_0009788 category ThingWithTaxon @default.

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