assertion retraction graph subject predicate object datatype annotation 1 0 graph DOID:2730 oio:hasDbXref UMLS_CUI:C0014527 xsd:string 1 0 graph DOID:2730 oio:hasDbXref GARD:6359 xsd:string 1 0 graph DOID:2730 oio:hasDbXref SNOMEDCT_US_2023_03_01:205580008 xsd:string 1 0 graph DOID:2730 oio:hasDbXref ICD10CM:Q81 xsd:string 1 0 graph DOID:2730 oio:inSubset obo:doid#NCIthesaurus _IRI 1 0 graph DOID:2730 oio:inSubset obo:doid#DO_rare_slim _IRI 1 0 graph DOID:2730 rdfs:label epidermolysis bullosa xsd:string 1 0 graph DOID:2730 rdf:type owl:Class _IRI 1 0 graph DOID:2730 oio:hasDbXref MESH:D004820 xsd:string 1 0 graph DOID:2730 rdfs:subClassOf DOID:2731 _IRI 1 0 graph DOID:2730 oio:hasDbXref NCI:C67383 xsd:string 1 0 graph DOID:2730 oio:hasExactSynonym acantholysis bullosa @en 1 0 graph DOID:2730 oio:hasOBONamespace disease_ontology xsd:string 1 0 graph DOID:2730 oio:id DOID:2730 xsd:string 1 0 graph DOID:2730 IAO:0000115 A vesiculobullous skin disease that is characterized by formation of blisters with only minor skin trauma, which can cause widespread wounds, dehydration, electrolyte abnormalities, and severe infection, frequently develops_from mutations in connective tissue elements, including genes encoding keratin, collagen, and laminin. xsd:string "{""dce:type"":[{""datatype"":""_IRI"",""meta"":""owl:Axiom"",""object"":""obo:ECO_0007636""}],""oio:hasDbXref"":[{""datatype"":""xsd:string"",""meta"":""owl:Axiom"",""object"":""url:https://rarediseases.org/rare-diseases/epidermolysis-bullosa/""}]}"