@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP58010.RA50gmRazLfrqCVK3gxN-BTTD2ZHienJLsb4xTz39DT1c> .
@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:NP58010.RA50gmRazLfrqCVK3gxN-BTTD2ZHienJLsb4xTz39DT1c130_head {
  this: np:hasAssertion dgn-np:NP58010.RA50gmRazLfrqCVK3gxN-BTTD2ZHienJLsb4xTz39DT1c130_assertion;
    np:hasProvenance dgn-np:NP58010.RA50gmRazLfrqCVK3gxN-BTTD2ZHienJLsb4xTz39DT1c130_provenance;
    np:hasPublicationInfo dgn-np:NP58010.RA50gmRazLfrqCVK3gxN-BTTD2ZHienJLsb4xTz39DT1c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP58010.RA50gmRazLfrqCVK3gxN-BTTD2ZHienJLsb4xTz39DT1c130_assertion a np:Assertion .
  
  dgn-np:NP58010.RA50gmRazLfrqCVK3gxN-BTTD2ZHienJLsb4xTz39DT1c130_provenance a np:Provenance .
  
  dgn-np:NP58010.RA50gmRazLfrqCVK3gxN-BTTD2ZHienJLsb4xTz39DT1c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP58010.RA50gmRazLfrqCVK3gxN-BTTD2ZHienJLsb4xTz39DT1c130_assertion {
  miriam-gene:3119 a ncit:C16612 .
  
  lld:C0010054 a ncit:C7057 .
  
  dgn-gda:DGN9d9e686b8974fed4b44967b13bb7e8a5 sio:SIO_000628 miriam-gene:3119, lld:C0010054;
    a sio:SIO_001122 .
}

dgn-np:NP58010.RA50gmRazLfrqCVK3gxN-BTTD2ZHienJLsb4xTz39DT1c130_provenance {
  dgn-np:NP58010.RA50gmRazLfrqCVK3gxN-BTTD2ZHienJLsb4xTz39DT1c130_assertion dct:description
      "[ The association of APOE, DRB1, D6589 and TNFa alleles with risk of CHD suggest that these are candidate genes or linked to genes for CHD in this cohort of AAW. Our data supported elevated plasma Lp(a) as a potential risk factor in AAW; however, its role is still unclear. The premenopausal AAW in this sample had a higher than expected rate of metabolic syndrome, which was associated with DRB1 alleles.]. 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:15825968;
    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:NP58010.RA50gmRazLfrqCVK3gxN-BTTD2ZHienJLsb4xTz39DT1c130_publicationInfo {
  this: dct:created "2014-10-02T12:32:27+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" .
}