FRINK Linked Data Fragments server

Matches in Ubergraph for { <http://purl.obolibrary.org/obo/MONDO_0012866> ?p ?o ?g. }

• MONDO_0012866 disease_has_major_feature PATO_0000585 @default.
• MONDO_0012866 disease_has_major_feature PATO_0000587 @default.
• MONDO_0012866 disease_has_major_feature PATO_0000596 @default.
• MONDO_0012866 disease_has_major_feature PATO_0000639 @default.
• MONDO_0012866 disease_has_major_feature PATO_0000918 @default.
• MONDO_0012866 disease_has_major_feature PATO_0001241 @default.
• MONDO_0012866 disease_has_major_feature PATO_0001623 @default.
• MONDO_0012866 disease_has_major_feature PATO_0001710 @default.
• MONDO_0012866 disease_has_major_feature PATO_0002037 @default.
• MONDO_0012866 disease_has_major_feature PATO_0002290 @default.
• MONDO_0012866 disease_has_major_feature PATO_0002301 @default.
• MONDO_0012866 disease_has_major_feature PATO_0002303 @default.
• MONDO_0012866 disease_has_major_feature UPHENO_0001001 @default.
• MONDO_0012866 normalizedInformationContent "100" @default.
• MONDO_0012866 referenceCount "1" @default.
• MONDO_0012866 hasDbXref "DOID:0110786" @default.
• MONDO_0012866 hasDbXref "GARD:10538" @default.
• MONDO_0012866 hasDbXref "MESH:C567311" @default.
• MONDO_0012866 hasDbXref "OMIM:612319" @default.
• MONDO_0012866 hasDbXref "Orphanet:171629" @default.
• MONDO_0012866 hasDbXref "SCTID:764688002" @default.
• MONDO_0012866 hasDbXref "UMLS:C3496228" @default.
• MONDO_0012866 hasExactSynonym "FA2H hereditary spastic paraplegia" @default.
• MONDO_0012866 hasExactSynonym "SPG35" @default.
• MONDO_0012866 hasExactSynonym "autosomal recessive spastic paraplegia 35" @default.
• MONDO_0012866 hasExactSynonym "autosomal recessive spastic paraplegia type 35" @default.
• MONDO_0012866 hasExactSynonym "hereditary spastic paraplegia 35" @default.
• MONDO_0012866 hasExactSynonym "hereditary spastic paraplegia caused by mutation in FA2H" @default.
• MONDO_0012866 hasExactSynonym "hereditary spastic paraplegia type 35" @default.
• MONDO_0012866 hasExactSynonym "leukodystrophy, dysmyelinating and spastic paraparesis with or without dystonia" @default.
• MONDO_0012866 hasRelatedSynonym "leukodystrophy, dysmyelinating, and spastic paraparesis with or without dystonia" @default.
• MONDO_0012866 hasRelatedSynonym "spastic paraplegia 35, autosomal recessive" @default.
• MONDO_0012866 id "MONDO:0012866" @default.
• MONDO_0012866 inSubset gard_rare @default.
• MONDO_0012866 inSubset nord_rare @default.
• MONDO_0012866 inSubset ordo_disease @default.
• MONDO_0012866 inSubset orphanet_rare @default.
• MONDO_0012866 inSubset rare @default.
• MONDO_0012866 type Class @default.
• MONDO_0012866 isDefinedBy mondo.owl @default.
• MONDO_0012866 label "hereditary spastic paraplegia 35" @default.
• MONDO_0012866 subClassOf Bc632b11131a0e24f09e6f71624292503 @default.
• MONDO_0012866 subClassOf Bd94d35bc99211a0abe656aa7290fe4a5 @default.
• MONDO_0012866 subClassOf BFO_0000001 @default.
• MONDO_0012866 subClassOf BFO_0000002 @default.
• MONDO_0012866 subClassOf BFO_0000016 @default.
• MONDO_0012866 subClassOf BFO_0000017 @default.
• MONDO_0012866 subClassOf BFO_0000020 @default.
• MONDO_0012866 subClassOf COB_0000033 @default.
• MONDO_0012866 subClassOf COB_0000111 @default.
• MONDO_0012866 subClassOf COB_0000502 @default.
• MONDO_0012866 subClassOf MONDO_0000001 @default.
• MONDO_0012866 subClassOf MONDO_0002602 @default.
• MONDO_0012866 subClassOf MONDO_0003757 @default.
• MONDO_0012866 subClassOf MONDO_0003847 @default.
• MONDO_0012866 subClassOf MONDO_0005071 @default.
• MONDO_0012866 subClassOf MONDO_0005559 @default.
• MONDO_0012866 subClassOf MONDO_0006496 @default.
• MONDO_0012866 subClassOf MONDO_0012866 @default.
• MONDO_0012866 subClassOf MONDO_0017913 @default.
• MONDO_0012866 subClassOf MONDO_0017915 @default.
• MONDO_0012866 subClassOf MONDO_0019064 @default.
• MONDO_0012866 subClassOf MONDO_0024237 @default.
• MONDO_0012866 subClassOf MONDO_0700096 @default.
• MONDO_0012866 subClassOf OGMS_0000031 @default.
• MONDO_0012866 subClassOf PATO_0000001 @default.
• MONDO_0012866 equivalentClass B9713d98da803e94e6395b3882c946bce @default.
• MONDO_0012866 equivalentClass B9ed4c39d4440cf93051231637361cdec @default.
• MONDO_0012866 exactMatch C567311 @default.
• MONDO_0012866 exactMatch 764688002 @default.
• MONDO_0012866 exactMatch C3496228 @default.
• MONDO_0012866 exactMatch DOID_0110786 @default.
• MONDO_0012866 exactMatch Orphanet_171629 @default.
• MONDO_0012866 exactMatch 612319 @default.
• MONDO_0012866 category Attribute @default.
• MONDO_0012866 category BiologicalEntity @default.
• MONDO_0012866 category Disease @default.
• MONDO_0012866 category DiseaseOrPhenotypicFeature @default.
• MONDO_0012866 category Entity @default.
• MONDO_0012866 category NamedThing @default.
• MONDO_0012866 category OntologyClass @default.
• MONDO_0012866 category OrganismAttribute @default.
• MONDO_0012866 category PhenotypicQuality @default.
• MONDO_0012866 category ThingWithTaxon @default.

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