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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#
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
n2:DOID_3883
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_0050736 n2:DOID_225 _:vb50952421
rdfs:label
Lynch syndrome
rdfs:comment
OMIM mapping confirmed by DO. [SN].
wdrs:describedby
n7:doid.owl
obo:id
DOID:3883
obo:hasAlternativeId
DOID:0050586 DOID:3040
obo:hasDbXref
GARD:9905 UMLS_CUI:C0009405 ORDO:144 NCI:C120083 MESH:D003123 OMIM:PS120435 UMLS_CUI:C1333990 SNOMEDCT_US_2021_09_01:315058005
obo:hasExactSynonym
hereditary nonpolyposis colorectal cancer hereditary nonpolyposis colorectal neoplasm Hereditary Defective Mismatch Repair syndrome COCA 1 HNPCC - hereditary nonpolyposis colon cancer
obo:hasOBONamespace
disease_ontology
obo:inSubset
n8:DO_rare_slim n8:NCIthesaurus
n2:IAO_0000115
A syndrome that is characterized by an increased risk for colon cancer and cancers of the endometrium, ovary, stomach, small intestine, hepatobiliary tract, urinary tract, brain, and skin and has_material_basis_in mutation of mismatch repair genes that increases the risk of many types of cancers.
Subject Item
_:vb50952421
rdf:type
owl:Restriction
owl:onProperty
n2:IDO_0000664
owl:someValuesFrom
n2:GENO_0000147
wdrs:describedby
n7:doid.owl