@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP44451.RAnGWMJBxBeXX9vPlhuCH31DEiO3pvG_2fcGzvPbPLE8o> .
@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:NP44451.RAnGWMJBxBeXX9vPlhuCH31DEiO3pvG_2fcGzvPbPLE8o130_head {
  this: np:hasAssertion dgn-np:NP44451.RAnGWMJBxBeXX9vPlhuCH31DEiO3pvG_2fcGzvPbPLE8o130_assertion;
    np:hasProvenance dgn-np:NP44451.RAnGWMJBxBeXX9vPlhuCH31DEiO3pvG_2fcGzvPbPLE8o130_provenance;
    np:hasPublicationInfo dgn-np:NP44451.RAnGWMJBxBeXX9vPlhuCH31DEiO3pvG_2fcGzvPbPLE8o130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP44451.RAnGWMJBxBeXX9vPlhuCH31DEiO3pvG_2fcGzvPbPLE8o130_assertion a np:Assertion .
  
  dgn-np:NP44451.RAnGWMJBxBeXX9vPlhuCH31DEiO3pvG_2fcGzvPbPLE8o130_provenance a np:Provenance .
  
  dgn-np:NP44451.RAnGWMJBxBeXX9vPlhuCH31DEiO3pvG_2fcGzvPbPLE8o130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP44451.RAnGWMJBxBeXX9vPlhuCH31DEiO3pvG_2fcGzvPbPLE8o130_assertion {
  miriam-gene:2153 a ncit:C16612 .
  
  lld:C1956346 a ncit:C7057 .
  
  dgn-gda:DGN77e8c15c67764264b0b41d40e2792594 sio:SIO_000628 miriam-gene:2153, lld:C1956346;
    a sio:SIO_001122 .
}

dgn-np:NP44451.RAnGWMJBxBeXX9vPlhuCH31DEiO3pvG_2fcGzvPbPLE8o130_provenance {
  dgn-np:NP44451.RAnGWMJBxBeXX9vPlhuCH31DEiO3pvG_2fcGzvPbPLE8o130_assertion dct:description
      "[Although both the heterozygote Factor VLeiden and Prothrombin gene mutations were more frequent in patients with CAD than in control subjects, there was no statistical relationship found to exist between coronary artery disease and the Factor VLeiden and]. 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:18452260;
    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:NP44451.RAnGWMJBxBeXX9vPlhuCH31DEiO3pvG_2fcGzvPbPLE8o130_publicationInfo {
  this: dct:created "2014-10-02T12:32:20+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" .
}