{"@context":{"obo_purl":"http://purl.obolibrary.org/obo/","rdf":"http://www.w3.org/1999/02/22-rdf-syntax-ns#","owl":"http://www.w3.org/2002/07/owl#","rdfs":"http://www.w3.org/2000/01/rdf-schema#","metadata_def":"http://data.bioontology.org/metadata/def/","oboinowl_gen":"http://www.geneontology.org/formats/oboInOwl#","metadata":"http://data.bioontology.org/metadata/"},"@graph":[{"@id":"obo_purl:CHEBI_35341","@type":"owl:Class","rdfs:subClassOf":[{"@id":"obo_purl:CHEBI_18059"},{"@id":"obo_purl:CHEBI_51958"}],"metadata:def/mappingSameURI":{"@id":"obo_purl:CHEBI_35341"},"metadata:def/mappingLoom":"steroid","metadata:def/prefLabel":"steroid","obo_purl:IAO_0000115":["Any of naturally occurring compounds and synthetic analogues, based on the cyclopenta[a]phenanthrene carbon skeleton, partially or completely hydrogenated; there are usually methyl groups at C-10 and C-13, and often an alkyl group at C-17. By extension, one or more bond scissions, ring expansions and/or ring contractions of the skeleton may have occurred. Natural steroids are derived biogenetically from squalene, so may be considered as triterpenoids.","Any of naturally occurring compounds and synthetic analogues, based on the cyclopenta[a]phenanthrene carbon skeleton, partially or completely hydrogenated; there are usually methyl groups at C-10 and C-13, and often an alkyl group at C-17. By extension, one or more bond scissions, ring expansions and/or ring contractions of the skeleton may have occurred. Natural steroids are derived biogenetically from squalene which is a triterpene."],"oboinowl_gen:hasExactSynonym":["Steroid","steroids"],"metadata:prefixIRI":["CHEBI:35341","obo1:CHEBI_35341"],"rdfs:label":"steroid","oboinowl_gen:hasRelatedSynonym":"a steroid"},{"@id":"obo_purl:CHEBI_35350","rdfs:subClassOf":{"@id":"obo_purl:CHEBI_35341"}}]}