@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP752239.RA_Jc18BEks45DW6PfMKdQnIMLLHgFnAJomcxCUtpJBZ4> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP752239.RA_Jc18BEks45DW6PfMKdQnIMLLHgFnAJomcxCUtpJBZ4130_head {
  this: np:hasAssertion dgn-np:NP752239.RA_Jc18BEks45DW6PfMKdQnIMLLHgFnAJomcxCUtpJBZ4130_assertion;
    np:hasProvenance dgn-np:NP752239.RA_Jc18BEks45DW6PfMKdQnIMLLHgFnAJomcxCUtpJBZ4130_provenance;
    np:hasPublicationInfo dgn-np:NP752239.RA_Jc18BEks45DW6PfMKdQnIMLLHgFnAJomcxCUtpJBZ4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP752239.RA_Jc18BEks45DW6PfMKdQnIMLLHgFnAJomcxCUtpJBZ4130_assertion a np:Assertion .
  
  dgn-np:NP752239.RA_Jc18BEks45DW6PfMKdQnIMLLHgFnAJomcxCUtpJBZ4130_provenance a np:Provenance .
  
  dgn-np:NP752239.RA_Jc18BEks45DW6PfMKdQnIMLLHgFnAJomcxCUtpJBZ4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP752239.RA_Jc18BEks45DW6PfMKdQnIMLLHgFnAJomcxCUtpJBZ4130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  
  lld:C0034065 a ncit:C7057 .
  
  dgn-gda:DGN9cafc7ca712a8560ff2e3308a7e628b0 sio:SIO_000628 miriam-gene:4524, lld:C0034065;
    a sio:SIO_001121 .
}

dgn-np:NP752239.RA_Jc18BEks45DW6PfMKdQnIMLLHgFnAJomcxCUtpJBZ4130_provenance {
  dgn-np:NP752239.RA_Jc18BEks45DW6PfMKdQnIMLLHgFnAJomcxCUtpJBZ4130_assertion dcterms:description
      "[The FVL is statistically more frequent in patients with PE compared to the control group, and the frequency of FVL, FII, and MTHFR is not significantly higher in patients with acute PE who have no obvious risk factors compared to those with obvious risk factors.]. 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:19618008;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP752239.RA_Jc18BEks45DW6PfMKdQnIMLLHgFnAJomcxCUtpJBZ4130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:26+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}