SPARQL | HTML Microdata document
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Namespace Prefixes
Prefix IRI
n7 https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n5 http://purl.obolibrary.org/obo/
wdrs http://www.w3.org/2007/05/powder-s#
dc http://purl.org/dc/elements/1.1/
obo http://www.geneontology.org/formats/oboInOwl#
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#
Statements
Subject Item _:vb50945354
rdf:type
owl:Axiom
wdrs:describedby
n7:doid.owl
dc:type
n5:ECO_0007636
n5:ECO_0007645
owl:annotatedProperty
n5:IAO_0000115
owl:annotatedSource
n5:DOID_0111724
owl:annotatedTarget
A bone development disease characterized by short-limb dwarfism, brachydactyly, cardiac valvular disease, characteristic facial appearance, skin thickening, and laryngotracheal stenosis.
obo:hasDbXref
url:https://ghr.nlm.nih.gov/condition/geleophysic-dysplasia
url:https://www.ncbi.nlm.nih.gov/pubmed/31516831
url:https://www.ncbi.nlm.nih.gov/pubmed/20301776