@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP180708.RA8t5a--ZoiS1yXO0uINiJM2Xx6dvcPvmcMWRZLTdCwuY> .
@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:NP180708.RA8t5a--ZoiS1yXO0uINiJM2Xx6dvcPvmcMWRZLTdCwuY130_head {
  this: np:hasAssertion dgn-np:NP180708.RA8t5a--ZoiS1yXO0uINiJM2Xx6dvcPvmcMWRZLTdCwuY130_assertion;
    np:hasProvenance dgn-np:NP180708.RA8t5a--ZoiS1yXO0uINiJM2Xx6dvcPvmcMWRZLTdCwuY130_provenance;
    np:hasPublicationInfo dgn-np:NP180708.RA8t5a--ZoiS1yXO0uINiJM2Xx6dvcPvmcMWRZLTdCwuY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP180708.RA8t5a--ZoiS1yXO0uINiJM2Xx6dvcPvmcMWRZLTdCwuY130_assertion a np:Assertion .
  
  dgn-np:NP180708.RA8t5a--ZoiS1yXO0uINiJM2Xx6dvcPvmcMWRZLTdCwuY130_provenance a np:Provenance .
  
  dgn-np:NP180708.RA8t5a--ZoiS1yXO0uINiJM2Xx6dvcPvmcMWRZLTdCwuY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP180708.RA8t5a--ZoiS1yXO0uINiJM2Xx6dvcPvmcMWRZLTdCwuY130_assertion {
  miriam-gene:183 a ncit:C16612 .
  
  lld:C1956346 a ncit:C7057 .
  
  dgn-gda:DGN0aedfbe5186aededf9abd3c8b322b030 sio:SIO_000628 miriam-gene:183, lld:C1956346;
    a sio:SIO_001121 .
}

dgn-np:NP180708.RA8t5a--ZoiS1yXO0uINiJM2Xx6dvcPvmcMWRZLTdCwuY130_provenance {
  dgn-np:NP180708.RA8t5a--ZoiS1yXO0uINiJM2Xx6dvcPvmcMWRZLTdCwuY130_assertion dcterms:description
      "[The homozygous deletion allele (DD) of the angiotensin-I converting enzyme (ACE) gene and the T235 homozygote of the angiotensinogen (AGT) gene have been reported to be correlated with an increased prevalence of coronary artery disease (CAD) and myocardial infarction (MI).]. 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:9254851;
    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:NP180708.RA8t5a--ZoiS1yXO0uINiJM2Xx6dvcPvmcMWRZLTdCwuY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:38+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" .
}