@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP59577.RA2xwIV94i6hnWV58YrKywFlyO64lNV_S-2kfL57ZjZtI> .
@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 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:NP59577.RA2xwIV94i6hnWV58YrKywFlyO64lNV_S-2kfL57ZjZtI130_head {
  this: np:hasAssertion dgn-np:NP59577.RA2xwIV94i6hnWV58YrKywFlyO64lNV_S-2kfL57ZjZtI130_assertion;
    np:hasProvenance dgn-np:NP59577.RA2xwIV94i6hnWV58YrKywFlyO64lNV_S-2kfL57ZjZtI130_provenance;
    np:hasPublicationInfo dgn-np:NP59577.RA2xwIV94i6hnWV58YrKywFlyO64lNV_S-2kfL57ZjZtI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP59577.RA2xwIV94i6hnWV58YrKywFlyO64lNV_S-2kfL57ZjZtI130_assertion a np:Assertion .
  
  dgn-np:NP59577.RA2xwIV94i6hnWV58YrKywFlyO64lNV_S-2kfL57ZjZtI130_provenance a np:Provenance .
  
  dgn-np:NP59577.RA2xwIV94i6hnWV58YrKywFlyO64lNV_S-2kfL57ZjZtI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP59577.RA2xwIV94i6hnWV58YrKywFlyO64lNV_S-2kfL57ZjZtI130_assertion {
  miriam-gene:345 a ncit:C16612 .
  
  lld:C0027051 a ncit:C7057 .
  
  dgn-gda:DGN0a82520402bfa45d3dd1545ab7e45948 sio:SIO_000628 miriam-gene:345, lld:C0027051;
    a sio:SIO_001122 .
}

dgn-np:NP59577.RA2xwIV94i6hnWV58YrKywFlyO64lNV_S-2kfL57ZjZtI130_provenance {
  dgn-np:NP59577.RA2xwIV94i6hnWV58YrKywFlyO64lNV_S-2kfL57ZjZtI130_assertion dct:description
      "[ In this prospective study of apparently healthy middle-aged US men, carriers of the X1-S2 haplotype in the APOA1 XmnI and APOC3 SstI variants across the APOA1/C3/A4 gene cluster had higher TG levels, but there was no evidence for significant associations between these two common variants or haplotypes defined by them and risk of incident MI in this cohort.]. 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:15488874;
    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:NP59577.RA2xwIV94i6hnWV58YrKywFlyO64lNV_S-2kfL57ZjZtI130_publicationInfo {
  this: dct:created "2014-10-02T12:32:28+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}