{ "items" : [
    { "id" : "http://webisa.webdatacommons.org/206431654"
      "properties" : {
        "http://www.w3.org/1999/02/22-rdf-syntax-ns#type" : [ "http://www.w3.org/ns/prov#Entity" ] ,
        "http://www.w3.org/ns/prov#value" : [ "???premarketing and post-marketing regulatory controls.??? Under the FD&C Act, a medical device is:An instrument, apparatus, implement, machine, contrivance, implant, in vitro reagent, or other similar or related article, including a component part, or accessory which is:recognized in the official National Formulary, or the United States Pharmacopoeia, or any supplement to them,intended for use in" ] ,
        "http://www.w3.org/ns/prov#wasQuotedFrom" : [ "americanbar.org" ] } },

    { "id" : "http://webisa.webdatacommons.org/prov/24986075"
      "properties" : {
        "http://www.w3.org/ns/prov#wasDerivedFrom" : [ "http://webisa.webdatacommons.org/206431654"] } } }
