@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP191009.RAbn6JB8jdT1r9aS6vO7d1IlkO_v7Zr-rlq8Vru8SxdTc> .
@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:NP191009.RAbn6JB8jdT1r9aS6vO7d1IlkO_v7Zr-rlq8Vru8SxdTc130_head {
  this: np:hasAssertion dgn-np:NP191009.RAbn6JB8jdT1r9aS6vO7d1IlkO_v7Zr-rlq8Vru8SxdTc130_assertion;
    np:hasProvenance dgn-np:NP191009.RAbn6JB8jdT1r9aS6vO7d1IlkO_v7Zr-rlq8Vru8SxdTc130_provenance;
    np:hasPublicationInfo dgn-np:NP191009.RAbn6JB8jdT1r9aS6vO7d1IlkO_v7Zr-rlq8Vru8SxdTc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP191009.RAbn6JB8jdT1r9aS6vO7d1IlkO_v7Zr-rlq8Vru8SxdTc130_assertion a np:Assertion .
  
  dgn-np:NP191009.RAbn6JB8jdT1r9aS6vO7d1IlkO_v7Zr-rlq8Vru8SxdTc130_provenance a np:Provenance .
  
  dgn-np:NP191009.RAbn6JB8jdT1r9aS6vO7d1IlkO_v7Zr-rlq8Vru8SxdTc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP191009.RAbn6JB8jdT1r9aS6vO7d1IlkO_v7Zr-rlq8Vru8SxdTc130_assertion {
  miriam-gene:183 a ncit:C16612 .
  
  lld:C0149721 a ncit:C7057 .
  
  dgn-gda:DGN8412940f9981e9b4843fbefa06acf3ed sio:SIO_000628 miriam-gene:183, lld:C0149721;
    a sio:SIO_001121 .
}

dgn-np:NP191009.RAbn6JB8jdT1r9aS6vO7d1IlkO_v7Zr-rlq8Vru8SxdTc130_provenance {
  dgn-np:NP191009.RAbn6JB8jdT1r9aS6vO7d1IlkO_v7Zr-rlq8Vru8SxdTc130_assertion dcterms:description
      "[Exciting new discoveries concerned with polymorphisms of genes coding for angiotensin converting enzyme (ACE) and angiotensinogen suggest that Ang II may be genetically associated with increased risk for myocardial infarction, hypertension and left ventricular hypertrophy.]. 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:8583476;
    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:NP191009.RAbn6JB8jdT1r9aS6vO7d1IlkO_v7Zr-rlq8Vru8SxdTc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:45+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" .
}