{ "items" : [
    { "id" : "http://purl.obolibrary.org/obo/RO_0003302"
      "properties" : {
        "http://www.w3.org/1999/02/22-rdf-syntax-ns#type" : [ "http://www.w3.org/2002/07/owl#ObjectProperty" ] ,
        "http://www.w3.org/2000/01/rdf-schema#subPropertyOf" : [ "http://purl.obolibrary.org/obo/RO_0002410" ] ,
        "http://www.w3.org/2000/01/rdf-schema#label" : [ "causes or contributes to condition" ] ,
        "http://www.w3.org/2000/01/rdf-schema#comment" : [ "Genetic variations can span any level of granularity from a full genome or genotype to an individual gene  or sequence alteration.  These variations can be represented at the physical level (DNA/RNA macromolecules or their parts, as in the ChEBI ontology and Molecular Sequence Ontology) or at the abstract level (generically dependent continuant sequence features that are carried by these macromolecules, as in the Sequence Ontology and Genotype Ontology).  The causal relations in this hierarchy can be used in linking either physical or abstract genetic variations to phenotypes or diseases they cause or contribute to.\n\nEnvironmental exposures include those imposed by natural environments, experimentally applied conditions, or clinical interventions." ] ,
        "http://purl.obolibrary.org/obo/IAO_0000112" : [ "The genetic variant 'NM_007294.3(BRCA1):c.110C>A (p.Thr37Lys)' casues or contributes to the disease  'familial breast-ovarian cancer'.\n\nAn environment of exposure to arsenic causes or contributes to the phenotype of patchy skin hyperpigmentation, and the disease 'skin cancer'." ] ,
        "http://purl.obolibrary.org/obo/IAO_0000115" : [ "A relationship between an entity (e.g. a genotype, genetic variation, chemical, or environmental exposure) and a condition (a phenotype or disease), where the entity has some causal or contributing role that influences the condition." ] ,
        "http://purl.obolibrary.org/obo/IAO_0000116" : [ "Note that relationships of phenotypes to organisms/strains that bear them, or diseases they are manifest in, should continue to use RO:0002200 ! 'has phenotype' and RO:0002201 ! 'phenotype of'."] } } }
