@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP257821.RAFPLL0tBpKz1UnB0Ksv1Da-VzJu6xA7hlC_iewiDfYNk> .
@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:NP257821.RAFPLL0tBpKz1UnB0Ksv1Da-VzJu6xA7hlC_iewiDfYNk130_head {
  this: np:hasAssertion dgn-np:NP257821.RAFPLL0tBpKz1UnB0Ksv1Da-VzJu6xA7hlC_iewiDfYNk130_assertion;
    np:hasProvenance dgn-np:NP257821.RAFPLL0tBpKz1UnB0Ksv1Da-VzJu6xA7hlC_iewiDfYNk130_provenance;
    np:hasPublicationInfo dgn-np:NP257821.RAFPLL0tBpKz1UnB0Ksv1Da-VzJu6xA7hlC_iewiDfYNk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP257821.RAFPLL0tBpKz1UnB0Ksv1Da-VzJu6xA7hlC_iewiDfYNk130_assertion a np:Assertion .
  
  dgn-np:NP257821.RAFPLL0tBpKz1UnB0Ksv1Da-VzJu6xA7hlC_iewiDfYNk130_provenance a np:Provenance .
  
  dgn-np:NP257821.RAFPLL0tBpKz1UnB0Ksv1Da-VzJu6xA7hlC_iewiDfYNk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP257821.RAFPLL0tBpKz1UnB0Ksv1Da-VzJu6xA7hlC_iewiDfYNk130_assertion {
  miriam-gene:1636 a ncit:C16612 .
  
  lld:C0010054 a ncit:C7057 .
  
  dgn-gda:DGN27d49fe654bd828e4e312fd0e216badd sio:SIO_000628 miriam-gene:1636, lld:C0010054;
    a sio:SIO_001121 .
}

dgn-np:NP257821.RAFPLL0tBpKz1UnB0Ksv1Da-VzJu6xA7hlC_iewiDfYNk130_provenance {
  dgn-np:NP257821.RAFPLL0tBpKz1UnB0Ksv1Da-VzJu6xA7hlC_iewiDfYNk130_assertion dcterms:description
      "[In studies where the underlying odds ratios are determined to be homogeneous, the overall odds ratios for myocardial infarction and coronary artery disease with regard to the ACE DD genotype are estimated using the Mantel-Haenszel method.]. 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:10554703;
    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:NP257821.RAFPLL0tBpKz1UnB0Ksv1Da-VzJu6xA7hlC_iewiDfYNk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:24+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" .
}