<http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#R107>	<http://www.w3.org/2000/01/rdf-schema#range>	<http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C3910> .
<http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#R107>	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#ObjectProperty> .
<http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#R107>	<http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#P106>	"Conceptual Entity"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#R107>	<http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#P107>	"Has Cytogenetic Abnormality"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#R107>	<http://www.w3.org/2000/01/rdf-schema#domain>	<http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C7057> .
<http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#R107>	<http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#code>	"R107"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#R107>	<http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#P90>	"<n0:ComplexTerm xmlns:n0=\"http://ncicb.nci.nih.gov/xml/owl/EVS/ComplexProperties.xsd#\"><n0:term-name>Disease_Has_Cytogenetic_Abnormality</n0:term-name><n0:term-group>PT</n0:term-group><n0:term-source>NCI</n0:term-source></n0:ComplexTerm>" .
<http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#R107>	<http://www.w3.org/2000/01/rdf-schema#label>	"Disease_Has_Cytogenetic_Abnormality"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#R107>	<http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#P108>	"Disease_Has_Cytogenetic_Abnormality"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#R107>	<http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#P97>	"<n0:ComplexDefinition xmlns:n0=\"http://ncicb.nci.nih.gov/xml/owl/EVS/ComplexProperties.xsd#\"><n0:def-definition>A role used to relate a disease to the type of chromosomal abnormality present in the specified disease state. The domain and the range for this role are &#39;Disease, Disorder or Finding&#39; and &#39;Molecular Abnormality&#39;, respectively.</n0:def-definition><n0:def-source>NCI</n0:def-source></n0:ComplexDefinition>" .