<http://purl.obolibrary.org/obo/DOID_0110377>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0110377"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110377>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110377>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:H35.5"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110377>	<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_0110377>	<http://www.w3.org/2000/01/rdf-schema#label>	"retinitis pigmentosa 49"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110377>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A retinitis pigmentosa that has_material_basis_in mutation in the CNGA1 gene on chromosome 4p12."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110377>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"RP49"@en .
<http://purl.obolibrary.org/obo/DOID_0110377>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_10584> .
<http://purl.obolibrary.org/obo/DOID_0110377>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:613756"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110377>	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Class> .