@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP54545.RAq7j_HpVVT3FrtbvHfXvuG4uZ4jVheQFH0lgpO2dRNVk> .
@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:NP54545.RAq7j_HpVVT3FrtbvHfXvuG4uZ4jVheQFH0lgpO2dRNVk130_head {
  this: np:hasAssertion dgn-np:NP54545.RAq7j_HpVVT3FrtbvHfXvuG4uZ4jVheQFH0lgpO2dRNVk130_assertion;
    np:hasProvenance dgn-np:NP54545.RAq7j_HpVVT3FrtbvHfXvuG4uZ4jVheQFH0lgpO2dRNVk130_provenance;
    np:hasPublicationInfo dgn-np:NP54545.RAq7j_HpVVT3FrtbvHfXvuG4uZ4jVheQFH0lgpO2dRNVk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP54545.RAq7j_HpVVT3FrtbvHfXvuG4uZ4jVheQFH0lgpO2dRNVk130_assertion a np:Assertion .
  
  dgn-np:NP54545.RAq7j_HpVVT3FrtbvHfXvuG4uZ4jVheQFH0lgpO2dRNVk130_provenance a np:Provenance .
  
  dgn-np:NP54545.RAq7j_HpVVT3FrtbvHfXvuG4uZ4jVheQFH0lgpO2dRNVk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP54545.RAq7j_HpVVT3FrtbvHfXvuG4uZ4jVheQFH0lgpO2dRNVk130_assertion {
  miriam-gene:4313 a ncit:C16612 .
  
  lld:C0010054 a ncit:C7057 .
  
  dgn-gda:DGNf83849acfea03336e97ae93e5c4c7703 sio:SIO_000628 miriam-gene:4313, lld:C0010054;
    a sio:SIO_001122 .
}

dgn-np:NP54545.RAq7j_HpVVT3FrtbvHfXvuG4uZ4jVheQFH0lgpO2dRNVk130_provenance {
  dgn-np:NP54545.RAq7j_HpVVT3FrtbvHfXvuG4uZ4jVheQFH0lgpO2dRNVk130_assertion dcterms:description
      "[Incidence of haplotypes of four MMP-2 promoter polymorphisms (-1575G/A, -1306C/T, -790T/G and -735C/T) determined by PCR reactions with restriction analyses in 187 patients with coronary TVD (153 men, 34 women, age median 65 years) was compared to 196 control subjects without clinical signs of coronary heart disease (131 men and 65 women, age median 60 years).]. 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:14996438;
    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:NP54545.RAq7j_HpVVT3FrtbvHfXvuG4uZ4jVheQFH0lgpO2dRNVk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:25+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" .
}