HTML Microdata document

This HTML5 document contains 66 embedded RDF statements represented using HTML+Microdata notation.

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

Namespace Prefixes

Prefix	IRI
n5	http://linked.opendata.cz/resource/mesh/concept/
rdfs	http://www.w3.org/2000/01/rdf-schema#
rdf	http://www.w3.org/1999/02/22-rdf-syntax-ns#
n4	http://linked.opendata.cz/ontology/mesh/
owl	http://www.w3.org/2002/07/owl#
nci	http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
xsdh	http://www.w3.org/2001/XMLSchema#

Statements

Subject Item: nci:C3324
rdf:type: owl:Class
rdfs:label: Peutz-Jeghers Syndrome
owl:equivalentClass: _:vb637037
nci:P106: Disease or Syndrome
nci:P108: Peutz-Jeghers Syndrome
nci:P207: C0031269
nci:P325: <n0:ComplexDefinition xmlns:n0="http://ncicb.nci.nih.gov/xml/owl/EVS/ComplexProperties.xsd#"><n0:def-definition>A genetic disorder in which polyps form in the intestine and dark spots appear on the mouth and fingers. Having Peutz-Jeghers syndrome increases the risk of developing gastrointestinal and many other types of cancer.</n0:def-definition><n0:def-source>NCI-GLOSS</n0:def-source></n0:ComplexDefinition>
nci:P366: Peutz-Jeghers_Syndrome
nci:P90: <n0:ComplexTerm xmlns:n0="http://ncicb.nci.nih.gov/xml/owl/EVS/ComplexProperties.xsd#"><n0:term-name>PJS</n0:term-name><n0:term-group>PT</n0:term-group><n0:term-source>NCI-GLOSS</n0:term-source><n0:source-code>CDR0000377717</n0:source-code></n0:ComplexTerm> <n0:ComplexTerm xmlns:n0="http://ncicb.nci.nih.gov/xml/owl/EVS/ComplexProperties.xsd#"><n0:term-name>PJS</n0:term-name><n0:term-group>AB</n0:term-group><n0:term-source>NCI</n0:term-source></n0:ComplexTerm> <n0:ComplexTerm xmlns:n0="http://ncicb.nci.nih.gov/xml/owl/EVS/ComplexProperties.xsd#"><n0:term-name>Peutz-Jeghers syndrome</n0:term-name><n0:term-group>PT</n0:term-group><n0:term-source>NCI-GLOSS</n0:term-source><n0:source-code>CDR0000377716</n0:source-code></n0:ComplexTerm> <n0:ComplexTerm xmlns:n0="http://ncicb.nci.nih.gov/xml/owl/EVS/ComplexProperties.xsd#"><n0:term-name>Jeghers-Peutz Syndrome</n0:term-name><n0:term-group>SY</n0:term-group><n0:term-source>NCI</n0:term-source></n0:ComplexTerm> <n0:ComplexTerm xmlns:n0="http://ncicb.nci.nih.gov/xml/owl/EVS/ComplexProperties.xsd#"><n0:term-name>Peutz's Syndrome</n0:term-name><n0:term-group>SY</n0:term-group><n0:term-source>NCI</n0:term-source></n0:ComplexTerm> <n0:ComplexTerm xmlns:n0="http://ncicb.nci.nih.gov/xml/owl/EVS/ComplexProperties.xsd#"><n0:term-name>Peutz-Jeghers Syndrome</n0:term-name><n0:term-group>PT</n0:term-group><n0:term-source>NCI</n0:term-source></n0:ComplexTerm>
nci:P97: <n0:ComplexDefinition xmlns:n0="http://ncicb.nci.nih.gov/xml/owl/EVS/ComplexProperties.xsd#"><n0:def-definition>An inherited condition characterized by generalized hamartomatous multiple polyposis of the intestinal tract. Transmitted in an autosomal dominant fashion, Peutz-Jeghers syndrome consistently involves the jejunum and is associated with melanin spots of the lips, buccal mucosa, and fingers. This syndrome is associated with abnormalities of chromosome 19. Also known as Jeghers-Peutz syndrome and Peutz's syndrome. --2004</n0:def-definition><n0:def-source>NCI</n0:def-source></n0:ComplexDefinition>
nci:code: C3324
n4:hasConcept: n5:M0016441

Subject Item: _:vb637037
rdf:type: owl:Class
owl:intersectionOf: _:vb730893

Subject Item: _:vb702558
rdf:type: owl:Restriction
owl:onProperty: nci:R126
owl:someValuesFrom: nci:C4733

Subject Item: _:vb702559
rdf:type: owl:Restriction
owl:onProperty: nci:R106
owl:someValuesFrom: nci:C36695

Subject Item: _:vb702560
rdf:type: owl:Restriction
owl:onProperty: nci:R176
owl:someValuesFrom: nci:C18253

Subject Item: _:vb702561
rdf:type: owl:Restriction
owl:onProperty: nci:R116
owl:someValuesFrom: nci:C4872

Subject Item: _:vb702562
rdf:type: owl:Restriction
owl:onProperty: nci:R116
owl:someValuesFrom: nci:C9039

Subject Item: _:vb702563
rdf:type: owl:Restriction
owl:onProperty: nci:R116
owl:someValuesFrom: nci:C9063

Subject Item: _:vb702564
rdf:type: owl:Restriction
owl:onProperty: nci:R116
owl:someValuesFrom: nci:C4908

Subject Item: _:vb702565
rdf:type: owl:Restriction
owl:onProperty: nci:R116
owl:someValuesFrom: nci:C3850

Subject Item: _:vb702566
rdf:type: owl:Restriction
owl:onProperty: nci:R116
owl:someValuesFrom: nci:C7724

Subject Item: _:vb730893
rdf:first: nci:C3266
rdf:rest: _:vb780619

Subject Item: _:vb780619
rdf:first: _:vb702558
rdf:rest: _:vb780620

Subject Item: _:vb780620
rdf:first: _:vb702559
rdf:rest: _:vb780621

Subject Item: _:vb780621
rdf:first: _:vb702560
rdf:rest: _:vb780622

Subject Item: _:vb780622
rdf:first: _:vb702561
rdf:rest: _:vb780623

Subject Item: _:vb780623
rdf:first: _:vb702562
rdf:rest: _:vb780624

Subject Item: _:vb780624
rdf:first: _:vb702563
rdf:rest: _:vb780625

Subject Item: _:vb780625
rdf:first: _:vb702564
rdf:rest: _:vb780626

Subject Item: _:vb780626
rdf:first: _:vb702565
rdf:rest: _:vb780627

Subject Item: _:vb780627
rdf:first: _:vb702566
rdf:rest: rdf:nil