HTML Microdata document

This HTML5 document contains 72 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:C2892
rdf:type: owl:Class
rdfs:label: Nevoid Basal Cell Carcinoma Syndrome
owl:equivalentClass: _:vb629959
nci:P106: Disease or Syndrome
nci:P108: Nevoid Basal Cell Carcinoma Syndrome
nci:P207: C0004779
nci:P325: <n0:ComplexDefinition xmlns:n0="http://ncicb.nci.nih.gov/xml/owl/EVS/ComplexProperties.xsd#"><n0:def-definition>A genetic condition that causes unusual facial features and disorders of the skin, bones, nervous system, eyes, and endocrine glands. People with this syndrome have a higher risk of basal cell carcinoma.</n0:def-definition><n0:def-source>NCI-GLOSS</n0:def-source></n0:ComplexDefinition>
nci:P366: Basal_Cell_Nevus_Syndrome
nci:P90: <n0:ComplexTerm xmlns:n0="http://ncicb.nci.nih.gov/xml/owl/EVS/ComplexProperties.xsd#"><n0:term-name>Basal Cell Nevus 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>basal cell nevus syndrome</n0:term-name><n0:term-group>PT</n0:term-group><n0:term-source>NCI-GLOSS</n0:term-source><n0:source-code>CDR0000256555</n0:source-code></n0:ComplexTerm> <n0:ComplexTerm xmlns:n0="http://ncicb.nci.nih.gov/xml/owl/EVS/ComplexProperties.xsd#"><n0:term-name>Gorlin 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>Gorlin-Goltz 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>nevoid basal cell carcinoma syndrome</n0:term-name><n0:term-group>PT</n0:term-group><n0:term-source>NCI-GLOSS</n0:term-source><n0:source-code>CDR0000442897</n0:source-code></n0:ComplexTerm> <n0:ComplexTerm xmlns:n0="http://ncicb.nci.nih.gov/xml/owl/EVS/ComplexProperties.xsd#"><n0:term-name>Gorlin syndrome</n0:term-name><n0:term-group>PT</n0:term-group><n0:term-source>NCI-GLOSS</n0:term-source><n0:source-code>CDR0000322806</n0:source-code></n0:ComplexTerm> <n0:ComplexTerm xmlns:n0="http://ncicb.nci.nih.gov/xml/owl/EVS/ComplexProperties.xsd#"><n0:term-name>Nevoid Basal Cell Carcinoma 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 autosomal dominant genetic syndrome caused by abnormalities in the PTCH gene. It is characterized by multiple basal cell carcinomas at a young age, odontogenic keratocysts, and skeletal defects (bifurcated and splayed ribs, fusion of vertebrae, spinal bifida). Patients with this syndrome may also develop medulloblastomas and ovarian fibromas.</n0:def-definition><n0:def-source>NCI</n0:def-source></n0:ComplexDefinition>
nci:code: C2892
n4:hasConcept: n5:M0002195

Subject Item: _:vb629959
rdf:type: owl:Class
owl:intersectionOf: _:vb730686

Subject Item: _:vb649631
rdf:type: owl:Restriction
owl:onProperty: nci:R126
owl:someValuesFrom: nci:C2921

Subject Item: _:vb649632
rdf:type: owl:Restriction
owl:onProperty: nci:R108
owl:someValuesFrom: nci:C40465

Subject Item: _:vb649633
rdf:type: owl:Restriction
owl:onProperty: nci:R106
owl:someValuesFrom: nci:C36691

Subject Item: _:vb649634
rdf:type: owl:Restriction
owl:onProperty: nci:R176
owl:someValuesFrom: nci:C18255

Subject Item: _:vb649635
rdf:type: owl:Restriction
owl:onProperty: nci:R116
owl:someValuesFrom: nci:C4260

Subject Item: _:vb649636
rdf:type: owl:Restriction
owl:onProperty: nci:R116
owl:someValuesFrom: nci:C35268

Subject Item: _:vb649637
rdf:type: owl:Restriction
owl:onProperty: nci:R116
owl:someValuesFrom: nci:C3222

Subject Item: _:vb649638
rdf:type: owl:Restriction
owl:onProperty: nci:R116
owl:someValuesFrom: nci:C3498

Subject Item: _:vb649639
rdf:type: owl:Restriction
owl:onProperty: nci:R115
owl:someValuesFrom: nci:C6947

Subject Item: _:vb649640
rdf:type: owl:Restriction
owl:onProperty: nci:R115
owl:someValuesFrom: nci:C40461

Subject Item: _:vb730686
rdf:first: nci:C84348
rdf:rest: _:vb750168

Subject Item: _:vb750168
rdf:first: _:vb649631
rdf:rest: _:vb750169

Subject Item: _:vb750169
rdf:first: _:vb649632
rdf:rest: _:vb750170

Subject Item: _:vb750170
rdf:first: _:vb649633
rdf:rest: _:vb750171

Subject Item: _:vb750171
rdf:first: _:vb649634
rdf:rest: _:vb750172

Subject Item: _:vb750172
rdf:first: _:vb649635
rdf:rest: _:vb750173

Subject Item: _:vb750173
rdf:first: _:vb649636
rdf:rest: _:vb750174

Subject Item: _:vb750174
rdf:first: _:vb649637
rdf:rest: _:vb750175

Subject Item: _:vb750175
rdf:first: _:vb649638
rdf:rest: _:vb750176

Subject Item: _:vb750176
rdf:first: _:vb649639
rdf:rest: _:vb750177

Subject Item: _:vb750177
rdf:first: _:vb649640
rdf:rest: rdf:nil