FRINK Linked Data Fragments server

Matches in Ubergraph for { <http://purl.obolibrary.org/obo/MONDO_0014822> ?p ?o ?g. }

• MONDO_0014822 RO_0002320 NCBITaxon_9604 @default.
• MONDO_0014822 RO_0002320 NCBITaxon_9605 @default.
• MONDO_0014822 RO_0002320 NCBITaxon_9606 @default.
• MONDO_0014822 RO_0002320 OBI_0100026 @default.
• MONDO_0014822 RO_0002320 PCO_0000031 @default.
• MONDO_0014822 RO_0002410 CHR_9606-chr15q @default.
• MONDO_0014822 RO_0002410 CHR_9606-chr15q14 @default.
• MONDO_0014822 RO_0004017 CHR_9606-chr15q @default.
• MONDO_0014822 RO_0004017 CHR_9606-chr15q14 @default.
• MONDO_0014822 RO_0004019 CHR_9606-chr15q @default.
• MONDO_0014822 RO_0004019 CHR_9606-chr15q14 @default.
• MONDO_0014822 RO_0004023 CHR_9606-chr15q @default.
• MONDO_0014822 RO_0004023 CHR_9606-chr15q14 @default.
• MONDO_0014822 RO_0004030 CHR_9606-chr15q @default.
• MONDO_0014822 RO_0004030 CHR_9606-chr15q14 @default.
• MONDO_0014822 RO_0040035 CHR_9606-chr15q @default.
• MONDO_0014822 RO_0040035 CHR_9606-chr15q14 @default.
• MONDO_0014822 normalizedInformationContent "100" @default.
• MONDO_0014822 referenceCount "1" @default.
• MONDO_0014822 hasDbXref "GARD:17242" @default.
• MONDO_0014822 hasDbXref "OMIM:616898" @default.
• MONDO_0014822 hasDbXref "Orphanet:261190" @default.
• MONDO_0014822 hasDbXref "SCTID:719575008" @default.
• MONDO_0014822 hasDbXref "UMLS:C4225666" @default.
• MONDO_0014822 hasDbXref "UMLS:C4305230" @default.
• MONDO_0014822 hasExactSynonym "Del(15)(q14)" @default.
• MONDO_0014822 hasExactSynonym "monosomy 15q14" @default.
• MONDO_0014822 hasRelatedSynonym "chromosome 15q14 deletion syndrome" @default.
• MONDO_0014822 id "MONDO:0014822" @default.
• MONDO_0014822 inSubset gard_rare @default.
• MONDO_0014822 inSubset nord_rare @default.
• MONDO_0014822 inSubset ordo_malformation_syndrome @default.
• MONDO_0014822 inSubset orphanet_rare @default.
• MONDO_0014822 inSubset rare @default.
• MONDO_0014822 type Class @default.
• MONDO_0014822 isDefinedBy mondo.owl @default.
• MONDO_0014822 label "15q14 microdeletion syndrome" @default.
• MONDO_0014822 subClassOf B94cd785a6f9b8d7612f25f0facd58fdf @default.
• MONDO_0014822 subClassOf Bd9b430199ad0f632f63731a6e4b7a900 @default.
• MONDO_0014822 subClassOf BFO_0000001 @default.
• MONDO_0014822 subClassOf BFO_0000002 @default.
• MONDO_0014822 subClassOf BFO_0000016 @default.
• MONDO_0014822 subClassOf BFO_0000017 @default.
• MONDO_0014822 subClassOf BFO_0000020 @default.
• MONDO_0014822 subClassOf COB_0000033 @default.
• MONDO_0014822 subClassOf COB_0000111 @default.
• MONDO_0014822 subClassOf COB_0000502 @default.
• MONDO_0014822 subClassOf MONDO_0000001 @default.
• MONDO_0014822 subClassOf MONDO_0000761 @default.
• MONDO_0014822 subClassOf MONDO_0014822 @default.
• MONDO_0014822 subClassOf MONDO_0016913 @default.
• MONDO_0014822 subClassOf MONDO_0019040 @default.
• MONDO_0014822 subClassOf MONDO_0700096 @default.
• MONDO_0014822 subClassOf OGMS_0000031 @default.
• MONDO_0014822 subClassOf PATO_0000001 @default.
• MONDO_0014822 equivalentClass Bd02531f5a6e707b3476cec58b5096bd2 @default.
• MONDO_0014822 equivalentClass Bda68e0b3901906efe63b90fbdcd6ad40 @default.
• MONDO_0014822 exactMatch 719575008 @default.
• MONDO_0014822 exactMatch C4225666 @default.
• MONDO_0014822 exactMatch C4305230 @default.
• MONDO_0014822 exactMatch Orphanet_261190 @default.
• MONDO_0014822 exactMatch 616898 @default.
• MONDO_0014822 category Attribute @default.
• MONDO_0014822 category BiologicalEntity @default.
• MONDO_0014822 category Disease @default.
• MONDO_0014822 category DiseaseOrPhenotypicFeature @default.
• MONDO_0014822 category Entity @default.
• MONDO_0014822 category NamedThing @default.
• MONDO_0014822 category OntologyClass @default.
• MONDO_0014822 category OrganismAttribute @default.
• MONDO_0014822 category PhenotypicQuality @default.
• MONDO_0014822 category ThingWithTaxon @default.

• first
• previous