assertion retraction graph subject predicate object datatype annotation 1 0 graph DOID:11198 IAO:0000115 A syndrome that has_material_basis_in a large deletion of the chromosome 22q11.2 region which includes the DGS gene needed for development of the thymus and related glands with subsequent lack of T-cell production. xsd:string "{""dce:type"":[{""datatype"":""_IRI"",""meta"":""owl:Axiom"",""object"":""obo:ECO_0007643""},{""datatype"":""_IRI"",""meta"":""owl:Axiom"",""object"":""obo:ECO_0007646""}],""oio:hasDbXref"":[{""datatype"":""xsd:string"",""meta"":""owl:Axiom"",""object"":""url:http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gnd&part=digeorgesyndrome""},{""datatype"":""xsd:string"",""meta"":""owl:Axiom"",""object"":""url:https://ghr.nlm.nih.gov/condition/22q112-deletion-syndrome""}]}" 1 0 graph DOID:11198 oio:id DOID:11198 xsd:string 1 0 graph DOID:11198 oio:hasDbXref NCI:C2989 xsd:string 1 0 graph DOID:11198 oio:hasDbXref ICD10CM:D82.1 xsd:string 1 0 graph DOID:11198 rdfs:comment OMIM mapping confirmed by DO. [SN]. xsd:string 1 0 graph DOID:11198 oio:inSubset obo:doid#DO_rare_slim _IRI 1 0 graph DOID:11198 rdfs:label DiGeorge syndrome xsd:string 1 0 graph DOID:11198 oio:hasDbXref OMIM:188400 xsd:string 1 0 graph DOID:11198 oio:hasDbXref GARD:10299 xsd:string 1 0 graph DOID:11198 oio:hasExactSynonym Pharyngeal pouch syndrome @en 1 0 graph DOID:11198 oio:hasDbXref ICD9CM:279.11 xsd:string 1 0 graph DOID:11198 oio:hasExactSynonym 22q11.2 deletion syndrome @en 1 0 graph DOID:11198 oio:hasDbXref SNOMEDCT_US_2023_03_01:190991007 xsd:string 1 0 graph DOID:11198 oio:hasExactSynonym DiGeorge sequence @en 1 0 graph DOID:11198 oio:inSubset obo:doid#NCIthesaurus _IRI 1 0 graph DOID:11198 oio:hasOBONamespace disease_ontology xsd:string 1 0 graph DOID:11198 rdf:type owl:Class _IRI 1 0 graph DOID:11198 rdfs:subClassOf DOID:0060388 _IRI 1 0 graph DOID:11198 rdfs:subClassOf DOID:0050736 _IRI 1 0 graph DOID:11198 oio:hasDbXref UMLS_CUI:C0012236 xsd:string