@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP44371.RAaJa8lxDFoUFFapyPMevSPl5gZm3E36JAWhvHLzoxbPA> .
@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:NP44371.RAaJa8lxDFoUFFapyPMevSPl5gZm3E36JAWhvHLzoxbPA130_head {
  this: np:hasAssertion dgn-np:NP44371.RAaJa8lxDFoUFFapyPMevSPl5gZm3E36JAWhvHLzoxbPA130_assertion;
    np:hasProvenance dgn-np:NP44371.RAaJa8lxDFoUFFapyPMevSPl5gZm3E36JAWhvHLzoxbPA130_provenance;
    np:hasPublicationInfo dgn-np:NP44371.RAaJa8lxDFoUFFapyPMevSPl5gZm3E36JAWhvHLzoxbPA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP44371.RAaJa8lxDFoUFFapyPMevSPl5gZm3E36JAWhvHLzoxbPA130_assertion a np:Assertion .
  
  dgn-np:NP44371.RAaJa8lxDFoUFFapyPMevSPl5gZm3E36JAWhvHLzoxbPA130_provenance a np:Provenance .
  
  dgn-np:NP44371.RAaJa8lxDFoUFFapyPMevSPl5gZm3E36JAWhvHLzoxbPA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP44371.RAaJa8lxDFoUFFapyPMevSPl5gZm3E36JAWhvHLzoxbPA130_assertion {
  miriam-gene:2153 a ncit:C16612 .
  
  lld:C0032914 a ncit:C7057 .
  
  dgn-gda:DGN4666379ed11b1b51f7f4a62943cce15f sio:SIO_000628 miriam-gene:2153, lld:C0032914;
    a sio:SIO_001122 .
}

dgn-np:NP44371.RAaJa8lxDFoUFFapyPMevSPl5gZm3E36JAWhvHLzoxbPA130_provenance {
  dgn-np:NP44371.RAaJa8lxDFoUFFapyPMevSPl5gZm3E36JAWhvHLzoxbPA130_assertion dcterms: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:NP44371.RAaJa8lxDFoUFFapyPMevSPl5gZm3E36JAWhvHLzoxbPA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:20+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" .
}