This HTML5 document contains 28 embedded RDF statements represented using HTML+Microdata notation.

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

Namespace Prefixes

PrefixIRI
n7https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n2http://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#
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
n2:DOID_0070270
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_3883 n2:DOID_0060388 _:vb50940046
rdfs:label
hereditary nonpolyposis colorectal cancer type 8
wdrs:describedby
n7:doid.owl
obo:id
DOID:0070270
obo:hasDbXref
OMIM:613244
obo:hasExactSynonym
HNPCC8
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
A Lynch syndrome that has_material_basis_in heterozygous deletion of the 3' part of the EPCAM gene and intergenic regions adjacent to the MSH2 gene on chromosome 2p21. This results in transcriptional read-through and silencing of MSH2 in tissues expressing EPCAM.
Subject Item
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rdf:type
owl:Class
owl:intersectionOf
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wdrs:describedby
n7:doid.owl
Subject Item
_:vb50940047
rdf:type
owl:Restriction
owl:onProperty
n2:IDO_0000664
owl:someValuesFrom
n2:SO_0000159
wdrs:describedby
n7:doid.owl
Subject Item
_:vb50940048
rdf:type
owl:Restriction
owl:onProperty
n2:IDO_0000664
owl:someValuesFrom
n2:SO_0000340
wdrs:describedby
n7:doid.owl
Subject Item
_:vb50940049
rdf:first
_:vb50940048
rdf:rest
rdf:nil
wdrs:describedby
n7:doid.owl
Subject Item
_:vb50940050
rdf:first
_:vb50940047
rdf:rest
_:vb50940049
wdrs:describedby
n7:doid.owl