@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP46633.RAiXFx3geaQT5A8klAHl1QRXf38MdEGYEh8q_xdvN7rjU> .
@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:NP46633.RAiXFx3geaQT5A8klAHl1QRXf38MdEGYEh8q_xdvN7rjU130_head {
  this: np:hasAssertion dgn-np:NP46633.RAiXFx3geaQT5A8klAHl1QRXf38MdEGYEh8q_xdvN7rjU130_assertion;
    np:hasProvenance dgn-np:NP46633.RAiXFx3geaQT5A8klAHl1QRXf38MdEGYEh8q_xdvN7rjU130_provenance;
    np:hasPublicationInfo dgn-np:NP46633.RAiXFx3geaQT5A8klAHl1QRXf38MdEGYEh8q_xdvN7rjU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP46633.RAiXFx3geaQT5A8klAHl1QRXf38MdEGYEh8q_xdvN7rjU130_assertion a np:Assertion .
  
  dgn-np:NP46633.RAiXFx3geaQT5A8klAHl1QRXf38MdEGYEh8q_xdvN7rjU130_provenance a np:Provenance .
  
  dgn-np:NP46633.RAiXFx3geaQT5A8klAHl1QRXf38MdEGYEh8q_xdvN7rjU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP46633.RAiXFx3geaQT5A8klAHl1QRXf38MdEGYEh8q_xdvN7rjU130_assertion {
  miriam-gene:1361 a ncit:C16612 .
  
  lld:C0032914 a ncit:C7057 .
  
  dgn-gda:DGNaff4e434a33415d1759881ee98e76e34 sio:SIO_000628 miriam-gene:1361, lld:C0032914;
    a sio:SIO_001122 .
}

dgn-np:NP46633.RAiXFx3geaQT5A8klAHl1QRXf38MdEGYEh8q_xdvN7rjU130_provenance {
  dgn-np:NP46633.RAiXFx3geaQT5A8klAHl1QRXf38MdEGYEh8q_xdvN7rjU130_assertion dct:description
      "[We found no differences in the prevalence of genetic risk factors of thrombosis in women with preeclampsia compared with controls, which makes it unlikely that these polymorphisms are risk factors for preeclampsia.]. 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:15333035;
    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:NP46633.RAiXFx3geaQT5A8klAHl1QRXf38MdEGYEh8q_xdvN7rjU130_publicationInfo {
  this: dct:created "2014-10-02T12:32:21+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" .
}