Matches in DBpedia 2014 for { <http://dbpedia.org/resource/Bart_syndrome> ?p ?o. }
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- Bart_syndrome abstract "Bart syndrome is a genetic disorder characterized by the association of congenital localized absence of skin, epidermolysis bullosa, lesions of the mouth mucosa, and dystrophic nails.".
- Bart_syndrome omim "132000".
- Bart_syndrome wikiPageID "21381829".
- Bart_syndrome wikiPageRevisionID "414421129".
- Bart_syndrome hasPhotoCollection Bart_syndrome.
- Bart_syndrome name "Bart syndrome".
- Bart_syndrome omim "132000".
- Bart_syndrome subject Category:Collagen_disease.
- Bart_syndrome subject Category:Genodermatoses.
- Bart_syndrome type Abstraction100002137.
- Bart_syndrome type Attribute100024264.
- Bart_syndrome type Condition113920835.
- Bart_syndrome type Disease114070360.
- Bart_syndrome type IllHealth114052046.
- Bart_syndrome type Illness114061805.
- Bart_syndrome type PathologicalState114051917.
- Bart_syndrome type PhysicalCondition114034177.
- Bart_syndrome type State100024720.
- Bart_syndrome type Disease.
- Bart_syndrome type Situation.
- Bart_syndrome comment "Bart syndrome is a genetic disorder characterized by the association of congenital localized absence of skin, epidermolysis bullosa, lesions of the mouth mucosa, and dystrophic nails.".
- Bart_syndrome label "Bart syndrome".
- Bart_syndrome sameAs m.05f5vpy.
- Bart_syndrome sameAs Q4865135.
- Bart_syndrome sameAs Q4865135.
- Bart_syndrome sameAs 137.
- Bart_syndrome sameAs Bart_syndrome.
- Bart_syndrome wasDerivedFrom Bart_syndrome?oldid=414421129.
- Bart_syndrome isPrimaryTopicOf Bart_syndrome.
- Bart_syndrome name "Bart syndrome".