FRINK Linked Data Fragments server

Matches in Ubergraph for { <http://purl.obolibrary.org/obo/MONDO_0009675> ?p ?o ?g. }

• MONDO_0009675 RO_0040035 UBERON_0001630 @default.
• MONDO_0009675 RO_0040035 UBERON_0002036 @default.
• MONDO_0009675 RO_0040035 UBERON_0002204 @default.
• MONDO_0009675 RO_0040035 UBERON_0002385 @default.
• MONDO_0009675 RO_0040035 UBERON_0004120 @default.
• MONDO_0009675 RO_0040035 UBERON_0005090 @default.
• MONDO_0009675 RO_0040035 UBERON_0010000 @default.
• MONDO_0009675 RO_0040035 UBERON_0011216 @default.
• MONDO_0009675 RO_0040035 UBERON_0014892 @default.
• MONDO_0009675 RO_0040035 UBERON_0018254 @default.
• MONDO_0009675 RO_0040035 UPHENO_0001001 @default.
• MONDO_0009675 normalizedInformationContent "100" @default.
• MONDO_0009675 referenceCount "1" @default.
• MONDO_0009675 hasDbXref "DOID:0110275" @default.
• MONDO_0009675 hasDbXref "GARD:1057" @default.
• MONDO_0009675 hasDbXref "MESH:C535895" @default.
• MONDO_0009675 hasDbXref "NCIT:C142079" @default.
• MONDO_0009675 hasDbXref "OMIM:253600" @default.
• MONDO_0009675 hasDbXref "Orphanet:267" @default.
• MONDO_0009675 hasDbXref "SCTID:715341003" @default.
• MONDO_0009675 hasExactSynonym "CAPN3 autosomal recessive limb-girdle muscular dystrophy" @default.
• MONDO_0009675 hasExactSynonym "LGMD2A" @default.
• MONDO_0009675 hasExactSynonym "Leyden-Moebius muscular dystrophy" @default.
• MONDO_0009675 hasExactSynonym "autosomal recessive limb-girdle muscular dystrophy caused by mutation in CAPN3" @default.
• MONDO_0009675 hasExactSynonym "autosomal recessive limb-girdle muscular dystrophy type 2A" @default.
• MONDO_0009675 hasExactSynonym "calpainopathy" @default.
• MONDO_0009675 hasExactSynonym "limb-girdle muscular dystrophy due to calpain deficiency" @default.
• MONDO_0009675 hasExactSynonym "limb-girdle muscular dystrophy type 2A" @default.
• MONDO_0009675 hasExactSynonym "muscular dystrophy, limb-girdle, autosomal recessive 1" @default.
• MONDO_0009675 hasExactSynonym "muscular dystrophy, limb-girdle, type 2A" @default.
• MONDO_0009675 hasExactSynonym "pelvofemoral muscular dystrophy" @default.
• MONDO_0009675 hasExactSynonym "primary calpainopathy" @default.
• MONDO_0009675 hasRelatedSynonym "LGMD2" @default.
• MONDO_0009675 hasRelatedSynonym "limb-girdle muscular dystrophy type 2" @default.
• MONDO_0009675 hasRelatedSynonym "muscular dystrophy limb girdle type 2A, erb type" @default.
• MONDO_0009675 hasRelatedSynonym "muscular dystrophy, Pelvofemoral" @default.
• MONDO_0009675 hasRelatedSynonym "muscular dystrophy, limb-girdle, type 2" @default.
• MONDO_0009675 hasRelatedSynonym "myositis, eosinophilic" @default.
• MONDO_0009675 id "MONDO:0009675" @default.
• MONDO_0009675 inSubset gard_rare @default.
• MONDO_0009675 inSubset nord_rare @default.
• MONDO_0009675 inSubset ordo_disease @default.
• MONDO_0009675 inSubset orphanet_rare @default.
• MONDO_0009675 inSubset rare @default.
• MONDO_0009675 type Class @default.
• MONDO_0009675 isDefinedBy mondo.owl @default.
• MONDO_0009675 label "autosomal recessive limb-girdle muscular dystrophy type 2A" @default.
• MONDO_0009675 subClassOf BFO_0000001 @default.
• MONDO_0009675 subClassOf BFO_0000002 @default.
• MONDO_0009675 subClassOf BFO_0000016 @default.
• MONDO_0009675 subClassOf BFO_0000017 @default.
• MONDO_0009675 subClassOf BFO_0000020 @default.
• MONDO_0009675 subClassOf COB_0000033 @default.
• MONDO_0009675 subClassOf COB_0000111 @default.
• MONDO_0009675 subClassOf COB_0000502 @default.
• MONDO_0009675 subClassOf MONDO_0000001 @default.
• MONDO_0009675 subClassOf MONDO_0000429 @default.
• MONDO_0009675 subClassOf MONDO_0002081 @default.
• MONDO_0009675 subClassOf MONDO_0003847 @default.
• MONDO_0009675 subClassOf MONDO_0003939 @default.
• MONDO_0009675 subClassOf MONDO_0005071 @default.
• MONDO_0009675 subClassOf MONDO_0005336 @default.
• MONDO_0009675 subClassOf MONDO_0006025 @default.
• MONDO_0009675 subClassOf MONDO_0009675 @default.
• MONDO_0009675 subClassOf MONDO_0015152 @default.
• MONDO_0009675 subClassOf MONDO_0016106 @default.
• MONDO_0009675 subClassOf MONDO_0016139 @default.
• MONDO_0009675 subClassOf MONDO_0016152 @default.
• MONDO_0009675 subClassOf MONDO_0016971 @default.
• MONDO_0009675 subClassOf MONDO_0019056 @default.
• MONDO_0009675 subClassOf MONDO_0020120 @default.
• MONDO_0009675 subClassOf MONDO_0020121 @default.
• MONDO_0009675 subClassOf MONDO_0700096 @default.
• MONDO_0009675 subClassOf MONDO_0700223 @default.
• MONDO_0009675 subClassOf OGMS_0000031 @default.
• MONDO_0009675 subClassOf PATO_0000001 @default.
• MONDO_0009675 equivalentClass B59bf0ac459a463f537419140ae24dd8e @default.
• MONDO_0009675 equivalentClass Bb501ff16b5ac746f3e46fb60061f9fc4 @default.
• MONDO_0009675 exactMatch NCIT_C142079 @default.
• MONDO_0009675 exactMatch C535895 @default.
• MONDO_0009675 exactMatch 715341003 @default.
• MONDO_0009675 exactMatch DOID_0110275 @default.
• MONDO_0009675 exactMatch Orphanet_267 @default.
• MONDO_0009675 exactMatch 253600 @default.
• MONDO_0009675 category Attribute @default.
• MONDO_0009675 category BiologicalEntity @default.
• MONDO_0009675 category Disease @default.
• MONDO_0009675 category DiseaseOrPhenotypicFeature @default.
• MONDO_0009675 category Entity @default.
• MONDO_0009675 category NamedThing @default.
• MONDO_0009675 category OntologyClass @default.
• MONDO_0009675 category OrganismAttribute @default.
• MONDO_0009675 category PhenotypicQuality @default.
• MONDO_0009675 category ThingWithTaxon @default.

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