[ {
  "@graph" : [ {
    "@id" : "http://identifiers.org/ncbigene/9197",
    "@type" : [ "http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C16612" ]
  }, {
    "@id" : "http://linkedlifedata.com/resource/umls/id/C0085580",
    "@type" : [ "http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C7057" ]
  }, {
    "@id" : "http://rdf.disgenet.org/gene-disease-association.ttl#DGN1ad9c57ee0ece2235e85f819f232a7f8",
    "@type" : [ "http://semanticscience.org/resource/SIO_001121" ],
    "http://semanticscience.org/resource/SIO_000628" : [ {
      "@id" : "http://identifiers.org/ncbigene/9197"
    }, {
      "@id" : "http://linkedlifedata.com/resource/umls/id/C0085580"
    } ]
  } ],
  "@id" : "http://rdf.disgenet.org/nanopublications.trig#NP799294.RAVFgKknfzpkewmk9uc4oDWYsP8BeARsLMlnDiDctRJmo130_assertion"
}, {
  "@graph" : [ {
    "@id" : "http://rdf.disgenet.org/nanopublications.trig#NP799294.RAVFgKknfzpkewmk9uc4oDWYsP8BeARsLMlnDiDctRJmo",
    "@type" : [ "http://www.nanopub.org/nschema#Nanopublication" ],
    "http://www.nanopub.org/nschema#hasAssertion" : [ {
      "@id" : "http://rdf.disgenet.org/nanopublications.trig#NP799294.RAVFgKknfzpkewmk9uc4oDWYsP8BeARsLMlnDiDctRJmo130_assertion"
    } ],
    "http://www.nanopub.org/nschema#hasProvenance" : [ {
      "@id" : "http://rdf.disgenet.org/nanopublications.trig#NP799294.RAVFgKknfzpkewmk9uc4oDWYsP8BeARsLMlnDiDctRJmo130_provenance"
    } ],
    "http://www.nanopub.org/nschema#hasPublicationInfo" : [ {
      "@id" : "http://rdf.disgenet.org/nanopublications.trig#NP799294.RAVFgKknfzpkewmk9uc4oDWYsP8BeARsLMlnDiDctRJmo130_publicationInfo"
    } ]
  }, {
    "@id" : "http://rdf.disgenet.org/nanopublications.trig#NP799294.RAVFgKknfzpkewmk9uc4oDWYsP8BeARsLMlnDiDctRJmo130_assertion",
    "@type" : [ "http://www.nanopub.org/nschema#Assertion" ]
  }, {
    "@id" : "http://rdf.disgenet.org/nanopublications.trig#NP799294.RAVFgKknfzpkewmk9uc4oDWYsP8BeARsLMlnDiDctRJmo130_provenance",
    "@type" : [ "http://www.nanopub.org/nschema#Provenance" ]
  }, {
    "@id" : "http://rdf.disgenet.org/nanopublications.trig#NP799294.RAVFgKknfzpkewmk9uc4oDWYsP8BeARsLMlnDiDctRJmo130_publicationInfo",
    "@type" : [ "http://www.nanopub.org/nschema#PublicationInfo" ]
  } ],
  "@id" : "http://rdf.disgenet.org/nanopublications.trig#NP799294.RAVFgKknfzpkewmk9uc4oDWYsP8BeARsLMlnDiDctRJmo130_head"
}, {
  "@graph" : [ {
    "@id" : "http://rdf.disgenet.org/nanopublications.trig#NP799294.RAVFgKknfzpkewmk9uc4oDWYsP8BeARsLMlnDiDctRJmo130_assertion",
    "http://purl.org/dc/terms/description" : [ {
      "@language" : "en",
      "@value" : "[Although polymorphisms in renin-angiotensin-aldosterone (RAA) system genes for angiotensinogen (AGT M235T), angiotensin-converting enzyme (ACE I/D), angiotensin II type 1 receptor (AT1 A/C1166), and aldosterone synthase (CYP11B2-344T/C) have been major targets for genetic investigation in association with essential hypertension (EH), the influence of these genetic factors is still to be determined.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."
    } ],
    "http://purl.org/ontology/wi/core#evidence" : [ {
      "@id" : "http://rdf.disgenet.org/v2.1.0/void.ttl#source_evidence_literature"
    } ],
    "http://semanticscience.org/resource/SIO_000772" : [ {
      "@id" : "http://identifiers.org/pubmed/17190732"
    } ],
    "http://www.w3.org/ns/prov#wasDerivedFrom" : [ {
      "@id" : "http://rdf.disgenet.org/v2.1.0/void.ttl#befree-20140225"
    } ],
    "http://www.w3.org/ns/prov#wasGeneratedBy" : [ {
      "@id" : "http://purl.obolibrary.org/obo/eco.owl#ECO_0000203"
    } ]
  }, {
    "@id" : "http://rdf.disgenet.org/v2.1.0/void.ttl#befree-20140225",
    "http://purl.org/pav/2.0/importedOn" : [ {
      "@type" : "http://www.w3.org/2001/XMLSchema#date",
      "@value" : "2014-02-25"
    } ]
  }, {
    "@id" : "http://rdf.disgenet.org/v2.1.0/void.ttl#source_evidence_literature",
    "@type" : [ "http://purl.obolibrary.org/obo/eco.owl#ECO_0000212" ],
    "http://www.w3.org/2000/01/rdf-schema#comment" : [ {
      "@language" : "en",
      "@value" : "Gene-disease associations inferred from text-mining the literature."
    } ],
    "http://www.w3.org/2000/01/rdf-schema#label" : [ {
      "@language" : "en",
      "@value" : "DisGeNET evidence - LITERATURE"
    } ]
  } ],
  "@id" : "http://rdf.disgenet.org/nanopublications.trig#NP799294.RAVFgKknfzpkewmk9uc4oDWYsP8BeARsLMlnDiDctRJmo130_provenance"
}, {
  "@graph" : [ {
    "@id" : "http://rdf.disgenet.org/nanopublications.trig#NP799294.RAVFgKknfzpkewmk9uc4oDWYsP8BeARsLMlnDiDctRJmo",
    "http://purl.org/dc/terms/created" : [ {
      "@type" : "http://www.w3.org/2001/XMLSchema#dateTime",
      "@value" : "2014-10-02T12:40:10+02:00"
    } ],
    "http://purl.org/dc/terms/rights" : [ {
      "@id" : "http://opendatacommons.org/licenses/odbl/1.0/"
    } ],
    "http://purl.org/dc/terms/rightsHolder" : [ {
      "@id" : "http://rdf.disgenet.org/v2.1.0/void.ttl#IBIGroup"
    } ],
    "http://purl.org/dc/terms/subject" : [ {
      "@id" : "http://semanticscience.org/resource/SIO_000983"
    } ],
    "http://purl.org/net/provenance/ns#usedData" : [ {
      "@id" : "http://rdf.disgenet.org/v2.1.0/void.ttl#disgenetrdf"
    } ],
    "http://purl.org/pav/2.0/authoredBy" : [ {
      "@id" : "http://orcid.org/0000-0001-5999-6269"
    }, {
      "@id" : "http://orcid.org/0000-0002-7534-7661"
    }, {
      "@id" : "http://orcid.org/0000-0002-9383-528X"
    }, {
      "@id" : "http://orcid.org/0000-0003-0169-8159"
    }, {
      "@id" : "http://orcid.org/0000-0003-1244-7654"
    } ],
    "http://purl.org/pav/2.0/createdBy" : [ {
      "@id" : "http://orcid.org/0000-0003-0169-8159"
    } ],
    "http://purl.org/pav/2.0/version" : [ {
      "@value" : "v2.1.0.0"
    } ]
  }, {
    "@id" : "http://rdf.disgenet.org/v2.1.0/void.ttl#disgenetrdf",
    "http://purl.org/pav/2.0/version" : [ {
      "@value" : "v2.1.0"
    } ]
  } ],
  "@id" : "http://rdf.disgenet.org/nanopublications.trig#NP799294.RAVFgKknfzpkewmk9uc4oDWYsP8BeARsLMlnDiDctRJmo130_publicationInfo"
} ]