This HTML5 document contains 92 embedded RDF statements represented using HTML+Microdata notation.

The embedded RDF content will be recognized by any processor of HTML5 Microdata.

Namespace Prefixes

PrefixIRI
dbpedia-dehttp://de.dbpedia.org/resource/
dctermshttp://purl.org/dc/terms/
yago-reshttp://yago-knowledge.org/resource/
dbohttp://dbpedia.org/ontology/
foafhttp://xmlns.com/foaf/0.1/
n19http://dbpedia.org/resource/Template:Transcription_factor/
n17https://global.dbpedia.org/id/
yagohttp://dbpedia.org/class/yago/
dbthttp://dbpedia.org/resource/Template:
rdfshttp://www.w3.org/2000/01/rdf-schema#
n16https://medlineplus.gov/genetics/condition/gillespie-syndrome/
freebasehttp://rdf.freebase.com/ns/
n6http://commons.wikimedia.org/wiki/Special:FilePath/
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
owlhttp://www.w3.org/2002/07/owl#
wikipedia-enhttp://en.wikipedia.org/wiki/
dbchttp://dbpedia.org/resource/Category:
dbphttp://dbpedia.org/property/
provhttp://www.w3.org/ns/prov#
xsdhhttp://www.w3.org/2001/XMLSchema#
wikidatahttp://www.wikidata.org/entity/
dbrhttp://dbpedia.org/resource/

Statements

Subject Item
dbr:Gillespie_syndrome
rdf:type
yago:PathologicalState114051917 yago:Disorder114052403 yago:Whole105869584 yago:PhysicalCondition114034177 yago:WikicatSyndromes wikidata:Q12136 owl:Thing yago:State100024720 yago:Concept105835747 yago:GeneticDisease114151139 yago:Abstraction100002137 yago:WikicatAutosomalDominantDisorders dbo:Disease yago:Condition113920835 yago:WikicatAutosomalRecessiveDisorders yago:Content105809192 yago:Complex105870365 yago:Idea105833840 yago:PsychologicalFeature100023100 yago:Syndrome105870790 yago:Disease114070360 yago:Illness114061805 yago:Attribute100024264 yago:Cognition100023271 yago:AutosomalDominantDisease114162025 yago:IllHealth114052046
rdfs:label
Gillespie-Syndrom Gillespie syndrome
rdfs:comment
Das Gillespie-Syndrom ist eine sehr seltene angeborene Erkrankung mit den Hauptmerkmalen Aniridie, zerebelläre Ataxie und Intelligenzminderung. Synonyme sind: Aniridie-zerebelläre Ataxie-Intelligenzminderung-Syndrom Die Erstbeschreibung stammt aus dem Jahre 1965 durch den US-amerikanischen Augenarzt Frederick D. Gillespie. Gillespie syndrome, also called aniridia, cerebellar ataxia and mental deficiency, is a rare genetic disorder. The disorder is characterized by partial aniridia (meaning that part of the iris is missing), ataxia (motor and coordination problems), and, in most cases, intellectual disability. It is heterogeneous, inherited in either an autosomal dominant or autosomal recessive manner. Gillespie syndrome was first described by American ophthalmologist Fredrick Gillespie in 1965.
foaf:name
Gillespie syndrome
dbp:name
Gillespie syndrome
foaf:depiction
n6:Autosomal_recessive_-_en.svg n6:Autosomal_dominant_-_en.svg
dcterms:subject
dbc:Syndromes_affecting_the_eye dbc:Syndromes_affecting_the_nervous_system dbc:Syndromes_with_intellectual_disability dbc:Rare_syndromes dbc:Autosomal_recessive_disorders dbc:Autosomal_dominant_disorders
dbo:wikiPageID
22264695
dbo:wikiPageRevisionID
1084515650
dbo:wikiPageWikiLink
dbc:Syndromes_affecting_the_eye dbc:Syndromes_affecting_the_nervous_system dbc:Syndromes_with_intellectual_disability dbr:Ataxia dbr:Genetic_disorder dbr:Iris_(anatomy) dbc:Autosomal_recessive_disorders dbc:Rare_syndromes dbr:Aniridia dbr:Chromosome_3 dbr:Genetic_carrier dbr:PAX6 dbr:Heterogeneity dbr:Intellectual_disability dbr:ITPR1 dbr:Autosome dbr:Ophthalmologist dbc:Autosomal_dominant_disorders dbr:Spinocerebellar_ataxia dbr:Dominance_(genetics)
dbo:wikiPageExternalLink
n16:
owl:sameAs
wikidata:Q5562120 yago-res:Gillespie_syndrome n17:4kCJu dbpedia-de:Gillespie-Syndrom freebase:m.05q471k
dbp:wikiPageUsesTemplate
dbt:Infobox_medical_condition_(new) dbt:Empty_section dbt:Reflist dbt:Cn n19:coregulator_deficiencies dbt:Medical_resources dbt:Multiple_image
dbo:thumbnail
n6:Autosomal_dominant_-_en.svg?width=300
dbp:diseasesdb
32735
dbp:icd
759.89 G11.05
dbp:omim
206700
dbp:orphanet
1065
dbp:synonyms
Aniridia-cerebellar ataxia-intellectual disability, Partial aniridia-cerebellar ataxia-oligophrenia
dbo:abstract
Das Gillespie-Syndrom ist eine sehr seltene angeborene Erkrankung mit den Hauptmerkmalen Aniridie, zerebelläre Ataxie und Intelligenzminderung. Synonyme sind: Aniridie-zerebelläre Ataxie-Intelligenzminderung-Syndrom Die Erstbeschreibung stammt aus dem Jahre 1965 durch den US-amerikanischen Augenarzt Frederick D. Gillespie. Gillespie syndrome, also called aniridia, cerebellar ataxia and mental deficiency, is a rare genetic disorder. The disorder is characterized by partial aniridia (meaning that part of the iris is missing), ataxia (motor and coordination problems), and, in most cases, intellectual disability. It is heterogeneous, inherited in either an autosomal dominant or autosomal recessive manner. Gillespie syndrome was first described by American ophthalmologist Fredrick Gillespie in 1965.
dbo:icd9
759.89
prov:wasDerivedFrom
wikipedia-en:Gillespie_syndrome?oldid=1084515650&ns=0
dbo:wikiPageLength
9679
dbo:diseasesDB
32735
dbo:icd10
G11.05
dbo:omim
206700
dbo:orpha
1065
foaf:isPrimaryTopicOf
wikipedia-en:Gillespie_syndrome