@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP48764.RAyRMMsWxC-u3g3SpqPTL5tAu55LfY3jQp6iTmC-Hsg3U> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP48764.RAyRMMsWxC-u3g3SpqPTL5tAu55LfY3jQp6iTmC-Hsg3U130_head {
  this: np:hasAssertion dgn-np:NP48764.RAyRMMsWxC-u3g3SpqPTL5tAu55LfY3jQp6iTmC-Hsg3U130_assertion;
    np:hasProvenance dgn-np:NP48764.RAyRMMsWxC-u3g3SpqPTL5tAu55LfY3jQp6iTmC-Hsg3U130_provenance;
    np:hasPublicationInfo dgn-np:NP48764.RAyRMMsWxC-u3g3SpqPTL5tAu55LfY3jQp6iTmC-Hsg3U130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP48764.RAyRMMsWxC-u3g3SpqPTL5tAu55LfY3jQp6iTmC-Hsg3U130_assertion a np:Assertion .
  
  dgn-np:NP48764.RAyRMMsWxC-u3g3SpqPTL5tAu55LfY3jQp6iTmC-Hsg3U130_provenance a np:Provenance .
  
  dgn-np:NP48764.RAyRMMsWxC-u3g3SpqPTL5tAu55LfY3jQp6iTmC-Hsg3U130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP48764.RAyRMMsWxC-u3g3SpqPTL5tAu55LfY3jQp6iTmC-Hsg3U130_assertion {
  miriam-gene:186 a ncit:C16612 .
  
  lld:C0020538 a ncit:C7057 .
  
  dgn-gda:DGN21d61cb01f17002565a0eda9ebb1f8d6 sio:SIO_000628 miriam-gene:186, lld:C0020538;
    a sio:SIO_001122 .
}

dgn-np:NP48764.RAyRMMsWxC-u3g3SpqPTL5tAu55LfY3jQp6iTmC-Hsg3U130_provenance {
  dgn-np:NP48764.RAyRMMsWxC-u3g3SpqPTL5tAu55LfY3jQp6iTmC-Hsg3U130_assertion dcterms:description
      "[This is the first study to demonstrate an association of AT2R genotype with coronary risk, an effect that was confined to hypertensive subjects and supports the concept that the inducible AT2R is protective. Conversely, the AT1R1166CC genotype was associated with cardiovascular risk irrespective of blood pressure. These data are important to our understanding of the divergent role of angiotensin II acting at its receptor subtypes and coronary disease pathogenesis and for the development of future cardiovascular therapies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:12925562;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^xsd:date .
  
  dgn-void:source_evidence_literature a eco:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP48764.RAyRMMsWxC-u3g3SpqPTL5tAu55LfY3jQp6iTmC-Hsg3U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:22+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}