<http://purl.obolibrary.org/obo/DOID_13910>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:13910"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_13910>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD9CM:368.51"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_13910>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:303900"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_13910>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C0155015"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_13910>	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
<http://purl.obolibrary.org/obo/DOID_13910>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"SNOMEDCT_US_2021_09_01:51445007"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_13910>	<http://www.w3.org/2000/01/rdf-schema#label>	"red color blindness"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_13910>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_13399> .
<http://purl.obolibrary.org/obo/DOID_13910>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Protan defect"@en .
<http://purl.obolibrary.org/obo/DOID_13910>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:D003117"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_13910>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Protanopia"@en .
<http://purl.obolibrary.org/obo/DOID_13910>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_13910>	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Class> .