This HTML5 document contains 21 embedded RDF statements represented using HTML+Microdata notation.

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Namespace Prefixes

PrefixIRI
n7https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n3http://purl.obolibrary.org/obo/
wdrshttp://www.w3.org/2007/05/powder-s#
rdfshttp://www.w3.org/2000/01/rdf-schema#
obohttp://www.geneontology.org/formats/oboInOwl#
n8http://purl.obolibrary.org/obo/doid#
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
owlhttp://www.w3.org/2002/07/owl#
xsdhhttp://www.w3.org/2001/XMLSchema#

Statements

Subject Item
n3:DOID_2222
rdf:type
owl:Class
rdfs:subClassOf
_:vb50950628 n3:DOID_0050737 n3:DOID_1247
rdfs:label
factor X deficiency
wdrs:describedby
n7:doid.owl
obo:id
DOID:2222
obo:hasDbXref
NCI:C131632 UMLS_CUI:C0015519 SNOMEDCT_US_2021_09_01:76642003 MESH:D005171 GARD:6404
obo:hasExactSynonym
Factor X deficiency disease, Stuart-Prower
obo:hasOBONamespace
disease_ontology
obo:inSubset
n8:NCIthesaurus
n3:IAO_0000115
A blood coagulation disease that is characterized by the partial or complete absence of factor X activity in the blood.
Subject Item
_:vb50950628
rdf:type
owl:Restriction
owl:onProperty
n3:IDO_0000664
owl:someValuesFrom
n3:GENO_0000148
wdrs:describedby
n7:doid.owl