@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP327049.RACDt-CvsdQ126htoEfS5XxUP-IeBD1qHmsY8ySaPt-mk> .
@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:NP327049.RACDt-CvsdQ126htoEfS5XxUP-IeBD1qHmsY8ySaPt-mk130_head {
  this: np:hasAssertion dgn-np:NP327049.RACDt-CvsdQ126htoEfS5XxUP-IeBD1qHmsY8ySaPt-mk130_assertion;
    np:hasProvenance dgn-np:NP327049.RACDt-CvsdQ126htoEfS5XxUP-IeBD1qHmsY8ySaPt-mk130_provenance;
    np:hasPublicationInfo dgn-np:NP327049.RACDt-CvsdQ126htoEfS5XxUP-IeBD1qHmsY8ySaPt-mk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP327049.RACDt-CvsdQ126htoEfS5XxUP-IeBD1qHmsY8ySaPt-mk130_assertion a np:Assertion .
  
  dgn-np:NP327049.RACDt-CvsdQ126htoEfS5XxUP-IeBD1qHmsY8ySaPt-mk130_provenance a np:Provenance .
  
  dgn-np:NP327049.RACDt-CvsdQ126htoEfS5XxUP-IeBD1qHmsY8ySaPt-mk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP327049.RACDt-CvsdQ126htoEfS5XxUP-IeBD1qHmsY8ySaPt-mk130_assertion {
  miriam-gene:183 a ncit:C16612 .
  
  lld:C2733225 a ncit:C7057 .
  
  dgn-gda:DGN6d3a49ee3d04701da0758235010c5d66 sio:SIO_000628 miriam-gene:183, lld:C2733225;
    a sio:SIO_001121 .
}

dgn-np:NP327049.RACDt-CvsdQ126htoEfS5XxUP-IeBD1qHmsY8ySaPt-mk130_provenance {
  dgn-np:NP327049.RACDt-CvsdQ126htoEfS5XxUP-IeBD1qHmsY8ySaPt-mk130_assertion dcterms:description
      "[To explore the role of the angiotensinogen (AGT) gene in coronary atherosclerosis and thrombosis, we studied the effect of the AGT M235T gene variant on plasma AGT levels and BP in patients with coronary artery disease and in the subgroup of survivors of myocardial infarction as compared with angiographically defined control subjects.]. 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:10097233;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP327049.RACDt-CvsdQ126htoEfS5XxUP-IeBD1qHmsY8ySaPt-mk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:11+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" .
}