<http://purl.obolibrary.org/obo/CHEBI_36141> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://www.w3.org/2002/07/owl#Class> . <http://purl.obolibrary.org/obo/CHEBI_36141> <http://www.w3.org/2000/01/rdf-schema#subClassOf> <http://purl.obolibrary.org/obo/CHEBI_3992> . <http://purl.obolibrary.org/obo/CHEBI_36141> <http://data.bioontology.org/metadata/def/mappingSameURI> <http://purl.obolibrary.org/obo/CHEBI_36141> . <http://purl.obolibrary.org/obo/CHEBI_36141> <http://data.bioontology.org/metadata/def/mappingLoom> "quinone" . <http://purl.obolibrary.org/obo/CHEBI_36141> <http://data.bioontology.org/metadata/def/prefLabel> "quinone" . <http://purl.obolibrary.org/obo/CHEBI_36141> <http://purl.obolibrary.org/obo/IAO_0000115> "Compounds having a fully conjugated cyclic dione structure, such as that of benzoquinones, derived from aromatic compounds by conversion of an even number of -CH= groups into -C(=O)- groups with any necessary rearrangement of double bonds (polycyclic and heterocyclic analogues are included)." . <http://purl.obolibrary.org/obo/CHEBI_36141> <http://data.bioontology.org/metadata/prefixIRI> "CHEBI:36141" . <http://purl.obolibrary.org/obo/CHEBI_36141> <http://www.w3.org/2000/01/rdf-schema#label> "quinone" . <http://purl.obolibrary.org/obo/CHEBI_36141> <http://purl.obolibrary.org/obo/IAO_0000412> <http://purl.obolibrary.org/obo/chebi.owl> . <http://purl.obolibrary.org/obo/CHEBI_25830> <http://www.w3.org/2000/01/rdf-schema#subClassOf> <http://purl.obolibrary.org/obo/CHEBI_36141> . <http://purl.obolibrary.org/obo/CHEBI_25481> <http://www.w3.org/2000/01/rdf-schema#subClassOf> <http://purl.obolibrary.org/obo/CHEBI_36141> . <http://purl.obolibrary.org/obo/CHEBI_22729> <http://www.w3.org/2000/01/rdf-schema#subClassOf> <http://purl.obolibrary.org/obo/CHEBI_36141> . <http://purl.obolibrary.org/obo/CHEBI_36141> <http://data.bioontology.org/metadata/def/mappingSameURI> <http://purl.obolibrary.org/obo/CHEBI_36141> .