@prefix activity: . @prefix address: . @prefix agency: . @prefix assay: . @prefix assayCategory: . @prefix assayTargetLink: . @prefix biopax3: . @prefix calbc: . @prefix calbc-group: . @prefix carrierLink: . @prefix certainAgreement: . @prefix chebi: . @prefix chembl: . @prefix chemicalCompound: . @prefix chemicalCompoundRecord: . @prefix clan: . @prefix clinicalResult: . @prefix clinicalStudy: . @prefix clinicaltrials: . @prefix company: . @prefix confidenceScore: . @prefix contact: . @prefix country: . @prefix cpath: . @prefix curationLookup: . @prefix dailymed: . @prefix dailymed-drugs: . @prefix dailymed-ingredient: . @prefix dailymed-instance: . @prefix databaseReference: . @prefix dc: . @prefix dc-term: . @prefix diseaseontology: . @prefix diseasome: . @prefix diseasome-diseases: . @prefix diseasome-gene: . @prefix diseasome-instance: . @prefix documentType: . @prefix dosageForm: . @prefix drug: . @prefix drugbank: . @prefix drugbank-proteinSequence: . @prefix drugCategory: . @prefix drugInteraction: . @prefix drugTarget: . @prefix eligibility: . @prefix entrez-gene: . @prefix entrez-goterm: . @prefix entrezgene: . @prefix enzymeLink: . @prefix externalIdentifier: . @prefix externalLink: . @prefix factforge: . @prefix family: . @prefix foaf: . @prefix formulation: . @prefix freebase: . @prefix gene-rif: . @prefix geneontology: . @prefix geneSequence: . @prefix hapmap: . @prefix indication: . @prefix intervention: . @prefix investigator: . @prefix label: . @prefix lhgdn: . @prefix lifeskim: . @prefix linkedct: . @prefix linkedct-condition: . @prefix linkedct-intervention: . @prefix literatureCitation: . @prefix lld: . @prefix location: . @prefix measurement: . @prefix meddraSideEffect: . @prefix mixture: . @prefix molecularSpecies: . @prefix molecule: . @prefix moleculeType: . @prefix ontotext: . @prefix organismSpecies: . @prefix outcomeAnalysis: . @prefix outcomeMeasure: . @prefix overallOfficial: . @prefix owl: . @prefix owlim: . @prefix packager: . @prefix participantFlow: . @prefix patent: . @prefix pfam: . @prefix phenotype: . @prefix pointOfContact: . @prefix price: . @prefix primaryOutcome: . @prefix product: . @prefix property: . @prefix proteinSequence: . @prefix pubmed: . @prefix pubmed-article: . @prefix pubmed-author: . @prefix pubmed-mesh: . @prefix pubmed-meshheading: . @prefix pubmed-qualifier: . @prefix rdf: . @prefix rdfs: . @prefix relationshipType: . @prefix relontology: . @prefix reportingGroup: . @prefix researchStem: . @prefix responsibleParty: . @prefix result: . @prefix resultsBaseline: . @prefix resultsMeasure: . @prefix resultsOutcome: . @prefix secondaryOutcome: . @prefix sideEffect: . @prefix sideEffectFrequency: . @prefix sider: . @prefix sider-drug: . @prefix skos: . @prefix skos-xl: . @prefix snp: . @prefix structureType: . @prefix studyMilestone: . @prefix studyParticipants: . @prefix studyPeriod: . @prefix substructure: . @prefix symptom: . @prefix synonym: . @prefix targetLink: . @prefix targetType: . @prefix taxonomy: . @prefix taxonomyClass: . @prefix taxonomyKingdom: . @prefix transporterLink: . @prefix umls: . @prefix umls-concept: . @prefix umls-label: . @prefix umls-semnetwork: . @prefix uniprot: . @prefix uniprot-protein: . @prefix uniprot-unstable: . @prefix xsd: . a owl:Class , owl:Class , owl:Class ; rdfs:comment """Definition: A physical entity whose structure is comprised of other physical entities bound to each other non-covalently, at least one of which is a macromolecule (e.g. protein, DNA, or RNA). Complexes must be stable enough to function as a biological unit; in general, the temporary association of an enzyme with its substrate(s) should not be considered or represented as a complex. A complex is the physical product of an interaction (complexAssembly) and is not itself considered an interaction. Comment: In general, complexes should not be defined recursively so that smaller complexes exist within larger complexes, i.e. a complex should not be a COMPONENT of another complex (see comments on the COMPONENT property). The boundaries on the size of complexes described by this class are not defined here, although elements of the cell as large and dynamic as, e.g., a mitochondrion would typically not be described using this class (later versions of this ontology may include a cellularComponent class to represent these). The strength of binding and the topology of the components cannot be described currently, but may be included in future versions of the ontology, depending on community need. Examples: Ribosome, RNA polymerase II. Other examples of this class include complexes of multiple protein monomers and complexes of proteins and small molecules."""^^xsd:string , """Definition: A physical entity whose structure is comprised of other physical entities bound to each other non-covalently, at least one of which is a macromolecule (e.g. protein, DNA, or RNA). Complexes must be stable enough to function as a biological unit; in general, the temporary association of an enzyme with its substrate(s) should not be considered or represented as a complex. A complex is the physical product of an interaction (complexAssembly) and is not itself considered an interaction. Comment: In general, complexes should not be defined recursively so that smaller complexes exist within larger complexes, i.e. a complex should not be a COMPONENT of another complex (see comments on the COMPONENT property). The boundaries on the size of complexes described by this class are not defined here, although elements of the cell as large and dynamic as, e.g., a mitochondrion would typically not be described using this class (later versions of this ontology may include a cellularComponent class to represent these). The strength of binding and the topology of the components cannot be described currently, but may be included in future versions of the ontology, depending on community need. Examples: Ribosome, RNA polymerase II. Other examples of this class include complexes of multiple protein monomers and complexes of proteins and small molecules."""^^xsd:string , """Definition: A physical entity whose structure is comprised of other physical entities bound to each other non-covalently, at least one of which is a macromolecule (e.g. protein, DNA, or RNA). Complexes must be stable enough to function as a biological unit; in general, the temporary association of an enzyme with its substrate(s) should not be considered or represented as a complex. A complex is the physical product of an interaction (complexAssembly) and is not itself considered an interaction. Comment: In general, complexes should not be defined recursively so that smaller complexes exist within larger complexes, i.e. a complex should not be a COMPONENT of another complex (see comments on the COMPONENT property). The boundaries on the size of complexes described by this class are not defined here, although elements of the cell as large and dynamic as, e.g., a mitochondrion would typically not be described using this class (later versions of this ontology may include a cellularComponent class to represent these). The strength of binding and the topology of the components cannot be described currently, but may be included in future versions of the ontology, depending on community need. Examples: Ribosome, RNA polymerase II. Other examples of this class include complexes of multiple protein monomers and complexes of proteins and small molecules."""^^xsd:string ; owl:disjointWith , , , , , , , , , , , ; rdfs:subClassOf , , .