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PrefixNamespace IRI
n14http://en.wikipedia.org/wiki/List_of_MeSH_codes_(C10)
n12http://caligraph.org/resource/Prader%E2%80%93
skoshttp://www.w3.org/2004/02/skos/core#
rdfshttp://www.w3.org/2000/01/rdf-schema#
n4http://en.wikipedia.org/wiki/Category:
n11http://caligraph.org/resource/Mowat%E2%80%93
n15http://en.wikipedia.org/wiki/List_of_MeSH_codes_(C16)
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
owlhttp://www.w3.org/2002/07/owl#
n7http://caligraph.org/ontology/MeSH_code_(C16)
clgohttp://caligraph.org/ontology/
n9http://caligraph.org/ontology/MeSH_code_(C10)
n8http://en.wikipedia.org/wiki/
provhttp://www.w3.org/ns/prov#
xsdhhttp://www.w3.org/2001/XMLSchema#
dbrhttp://dbpedia.org/resource/
clgrhttp://caligraph.org/resource/
Subject Item
clgr:1p36_deletion_syndrome
clgo:differentialDiagnosis
clgr:Angelman_syndrome
Subject Item
clgr:Angelman_syndrome
rdf:type
clgo:Fetal_abnormality n7: n9: clgo:Neurological_condition_or_disorder owl:NamedIndividual clgo:Rare_syndrome clgo:Genetic_disorder clgo:Learning_disability clgo:Skin_condition clgo:Disorder_causing_seizures clgo:Congenital_disorder clgo:Genodermatose clgo:Autosomal_monosomy_or_deletion clgo:Eponymous_disease clgo:Syndrome_affecting_the_nervous_system
rdfs:label
Angelman syndrome
owl:sameAs
dbr:Angelman_syndrome
prov:wasDerivedFrom
n4:Genodermatoses n8:Microdeletion_syndrome n8:Karyotype n8:List_of_neurological_conditions_and_disorders n8:Hypopigmentation n4:Learning_disabilities n8:Aneuploidy n8:Ubiquitin n8:List_of_eponymous_diseases n8:List_of_syndromes n4:Syndromes_affecting_the_nervous_system n4:Disorders_causing_seizures n4:Rare_syndromes n8:List_of_skin_conditions n8:List_of_genetic_disorders n8:SYNGAP1-related_intellectual_disability n14: n15: n8:List_of_congenital_disorders n8:Epigenetics_of_human_development n8:List_of_fetal_abnormalities n4:Autosomal_monosomies_and_deletions
skos:prefLabel
Angelman syndrome
skos:altLabel
angelman syndrome Angelman_syndrome Angelman syndrome (AS) Angelman Syndrome Angelman
clgo:differentialDiagnosis
clgr:Rett_syndrome n12:Willi_syndrome clgr:Autism_spectrum clgr:Cerebral_palsy
clgo:diseasesDB
712
clgo:geneReviewsId
NBK1144
clgo:geneReviewsName
Angelman Syndrome
clgo:icd10
Q93.5
clgo:icd9
759.89
clgo:medicalCause
clgr:Genetics
clgo:medicalDiagnosis
clgr:Genetic_testing
clgo:medlinePlus
007616
clgo:meshId
D017204
clgo:omim
105830
clgo:orpha
72
clgo:symptom
clgr:Intellectual_disability clgr:Microcephaly
clgo:treatment
clgr:Symptomatic_treatment
Subject Item
n11:Wilson_syndrome
clgo:differentialDiagnosis
clgr:Angelman_syndrome