@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP48912.RAAC5hMWAYdTTM1HFxv-kUVaMYuv1yjOhJP3NZSbtBHpQ> .
@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:NP48912.RAAC5hMWAYdTTM1HFxv-kUVaMYuv1yjOhJP3NZSbtBHpQ130_head {
  this: np:hasAssertion dgn-np:NP48912.RAAC5hMWAYdTTM1HFxv-kUVaMYuv1yjOhJP3NZSbtBHpQ130_assertion;
    np:hasProvenance dgn-np:NP48912.RAAC5hMWAYdTTM1HFxv-kUVaMYuv1yjOhJP3NZSbtBHpQ130_provenance;
    np:hasPublicationInfo dgn-np:NP48912.RAAC5hMWAYdTTM1HFxv-kUVaMYuv1yjOhJP3NZSbtBHpQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP48912.RAAC5hMWAYdTTM1HFxv-kUVaMYuv1yjOhJP3NZSbtBHpQ130_assertion a np:Assertion .
  
  dgn-np:NP48912.RAAC5hMWAYdTTM1HFxv-kUVaMYuv1yjOhJP3NZSbtBHpQ130_provenance a np:Provenance .
  
  dgn-np:NP48912.RAAC5hMWAYdTTM1HFxv-kUVaMYuv1yjOhJP3NZSbtBHpQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP48912.RAAC5hMWAYdTTM1HFxv-kUVaMYuv1yjOhJP3NZSbtBHpQ130_assertion {
  miriam-gene:183 a ncit:C16612 .
  
  lld:C0010072 a ncit:C7057 .
  
  dgn-gda:DGNd23c0279ff5a9b41e575ac008addd8d3 sio:SIO_000628 miriam-gene:183, lld:C0010072;
    a sio:SIO_001122 .
}

dgn-np:NP48912.RAAC5hMWAYdTTM1HFxv-kUVaMYuv1yjOhJP3NZSbtBHpQ130_provenance {
  dgn-np:NP48912.RAAC5hMWAYdTTM1HFxv-kUVaMYuv1yjOhJP3NZSbtBHpQ130_assertion dcterms:description
      "[To investigate the distribution frequencies of angiotensin-converting enzyme (ACE), angiotensinogen (AGT), angiotensin II I type receptor (AT1R) genotypes in Chinese, to find the relationships between polymorphisms of ACE, AGT and AT1R gene, and coronary artery thrombosis disease (CATD) and to study the interactions of themselves, PCR and PCR-RFLP techniques were performed to determine the genotypes of ACE, AGT and AT1R gene in CATD group (192 cases) and control group (110 cases).]. 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:15498133;
    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:NP48912.RAAC5hMWAYdTTM1HFxv-kUVaMYuv1yjOhJP3NZSbtBHpQ130_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" .
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