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Prefix	IRI
n7	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n2	http://purl.obolibrary.org/obo/
wdrs	http://www.w3.org/2007/05/powder-s#
rdfs	http://www.w3.org/2000/01/rdf-schema#
obo	http://www.geneontology.org/formats/oboInOwl#
n4	http://purl.obolibrary.org/obo/doid#
rdf	http://www.w3.org/1999/02/22-rdf-syntax-ns#
owl	http://www.w3.org/2002/07/owl#
xsdh	http://www.w3.org/2001/XMLSchema#

Subject Item: n2:DOID_1933
rdf:type: owl:Class
rdfs:subClassOf: _:vb50950339 n2:DOID_0050736 n2:DOID_0060388 _:vb50950334 n2:DOID_225
rdfs:label: Rubinstein-Taybi syndrome
rdfs:comment: Xref MGI. OMIM mapping confirmed by DO. [SN].
wdrs:describedby: n7:doid.owl
obo:id: DOID:1933
obo:hasDbXref: NCI:C75466 MESH:D012415 OMIM:610543 UMLS_CUI:C0035934 SNOMEDCT_US_2021_09_01:157032007 ORDO:783 ICD10CM:Q87.2 OMIM:613684 GARD:7593 OMIM:180849
obo:hasExactSynonym: Rubinstein syndrome Broad Thumb-Hallux syndrome proximal chromosome 16p13.3 deletion syndrome
obo:hasOBONamespace: disease_ontology
obo:inSubset: n4:NCIthesaurus n4:DO_rare_slim
n2:IAO_0000115: A syndrome characterized by short stature, moderate to sever intellectual disability, distinctive facial features and broad thumbs and first toes.