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Namespace Prefixes

PrefixIRI
n8https://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#
n6http://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_0050465
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_3883
rdfs:label
Muir-Torre syndrome
rdfs:comment
OMIM mapping confirmed by DO. [SN].
wdrs:describedby
n8:doid.owl
obo:id
DOID:0050465
obo:hasDbXref
MESH:D055653 SNOMEDCT_US_2021_09_01:403824007 GARD:6821 NCI:C84905 UMLS_CUI:C1321489 OMIM:158320
obo:hasOBONamespace
disease_ontology
obo:inSubset
n6:NCIthesaurus
n2:IAO_0000115
A Lynch syndrome that is characterized by a propensity to develop cancers of the gastrointestinal tract, genitourinary tract, and skin that has_material_basis_in mutations in DNA mismatch repair genes.