Matches in Ubergraph for { <http://purl.obolibrary.org/obo/MONDO_0010467> ?p ?o ?g. }
- MONDO_0010467 RO_0004017 CHR_9606-chrX @default.
- MONDO_0010467 RO_0004017 CHR_9606-chrXq @default.
- MONDO_0010467 RO_0004017 CHR_9606-chrXq27.3-q28 @default.
- MONDO_0010467 RO_0004019 CHR_9606-chrX @default.
- MONDO_0010467 RO_0004019 CHR_9606-chrXq @default.
- MONDO_0010467 RO_0004019 CHR_9606-chrXq27.3-q28 @default.
- MONDO_0010467 RO_0004023 CHR_9606-chrX @default.
- MONDO_0010467 RO_0004023 CHR_9606-chrXq @default.
- MONDO_0010467 RO_0004023 CHR_9606-chrXq27.3-q28 @default.
- MONDO_0010467 RO_0004030 CHR_9606-chrX @default.
- MONDO_0010467 RO_0004030 CHR_9606-chrXq @default.
- MONDO_0010467 RO_0004030 CHR_9606-chrXq27.3-q28 @default.
- MONDO_0010467 RO_0040035 CHR_9606-chrX @default.
- MONDO_0010467 RO_0040035 CHR_9606-chrXq @default.
- MONDO_0010467 RO_0040035 CHR_9606-chrXq27.3-q28 @default.
- MONDO_0010467 normalizedInformationContent "100" @default.
- MONDO_0010467 referenceCount "1" @default.
- MONDO_0010467 hasDbXref "GARD:17247" @default.
- MONDO_0010467 hasDbXref "OMIM:300869" @default.
- MONDO_0010467 hasDbXref "Orphanet:261483" @default.
- MONDO_0010467 hasDbXref "UMLS:C3275521" @default.
- MONDO_0010467 hasExactSynonym "Xq27.3-q28 microduplication syndrome" @default.
- MONDO_0010467 hasExactSynonym "chromosome xq27.3-q28 duplication syndrome, X-linked recessive" @default.
- MONDO_0010467 hasExactSynonym "dup(X)(q27.3q28)" @default.
- MONDO_0010467 hasExactSynonym "trisomy Xq27.3-q28" @default.
- MONDO_0010467 hasExactSynonym "trisomy Xq27.3q28" @default.
- MONDO_0010467 hasRelatedSynonym "chromosome Xq27.3-q28 DUPLICATION syndrome" @default.
- MONDO_0010467 id "MONDO:0010467" @default.
- MONDO_0010467 inSubset gard_rare @default.
- MONDO_0010467 inSubset nord_rare @default.
- MONDO_0010467 inSubset ordo_malformation_syndrome @default.
- MONDO_0010467 inSubset orphanet_rare @default.
- MONDO_0010467 inSubset rare @default.
- MONDO_0010467 type Class @default.
- MONDO_0010467 isDefinedBy mondo.owl @default.
- MONDO_0010467 label "Xq27.3q28 duplication syndrome" @default.
- MONDO_0010467 subClassOf B7def90e27caa0db0b27fa53068b8c364 @default.
- MONDO_0010467 subClassOf Be37d9b78e2de00e7002ed5d85bdfd95f @default.
- MONDO_0010467 subClassOf BFO_0000001 @default.
- MONDO_0010467 subClassOf BFO_0000002 @default.
- MONDO_0010467 subClassOf BFO_0000016 @default.
- MONDO_0010467 subClassOf BFO_0000017 @default.
- MONDO_0010467 subClassOf BFO_0000020 @default.
- MONDO_0010467 subClassOf COB_0000033 @default.
- MONDO_0010467 subClassOf COB_0000111 @default.
- MONDO_0010467 subClassOf COB_0000502 @default.
- MONDO_0010467 subClassOf MONDO_0000001 @default.
- MONDO_0010467 subClassOf MONDO_0000762 @default.
- MONDO_0010467 subClassOf MONDO_0010467 @default.
- MONDO_0010467 subClassOf MONDO_0017008 @default.
- MONDO_0010467 subClassOf MONDO_0017010 @default.
- MONDO_0010467 subClassOf MONDO_0019040 @default.
- MONDO_0010467 subClassOf MONDO_0020058 @default.
- MONDO_0010467 subClassOf MONDO_0700027 @default.
- MONDO_0010467 subClassOf MONDO_0700096 @default.
- MONDO_0010467 subClassOf OGMS_0000031 @default.
- MONDO_0010467 subClassOf PATO_0000001 @default.
- MONDO_0010467 equivalentClass B710884470744a5e08b07c921bf1baf49 @default.
- MONDO_0010467 equivalentClass B87b1c340e6159176888853feefccf5bf @default.
- MONDO_0010467 exactMatch C3275521 @default.
- MONDO_0010467 exactMatch Orphanet_261483 @default.
- MONDO_0010467 exactMatch 300869 @default.
- MONDO_0010467 category Attribute @default.
- MONDO_0010467 category BiologicalEntity @default.
- MONDO_0010467 category Disease @default.
- MONDO_0010467 category DiseaseOrPhenotypicFeature @default.
- MONDO_0010467 category Entity @default.
- MONDO_0010467 category NamedThing @default.
- MONDO_0010467 category OntologyClass @default.
- MONDO_0010467 category OrganismAttribute @default.
- MONDO_0010467 category PhenotypicQuality @default.
- MONDO_0010467 category ThingWithTaxon @default.