@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP855548.RAOjoFA_EDac62xPHDLy5swnpeYAMK-jWCnd2fvplsRfg> .
@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:NP855548.RAOjoFA_EDac62xPHDLy5swnpeYAMK-jWCnd2fvplsRfg130_head {
  this: np:hasAssertion dgn-np:NP855548.RAOjoFA_EDac62xPHDLy5swnpeYAMK-jWCnd2fvplsRfg130_assertion;
    np:hasProvenance dgn-np:NP855548.RAOjoFA_EDac62xPHDLy5swnpeYAMK-jWCnd2fvplsRfg130_provenance;
    np:hasPublicationInfo dgn-np:NP855548.RAOjoFA_EDac62xPHDLy5swnpeYAMK-jWCnd2fvplsRfg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP855548.RAOjoFA_EDac62xPHDLy5swnpeYAMK-jWCnd2fvplsRfg130_assertion a np:Assertion .
  
  dgn-np:NP855548.RAOjoFA_EDac62xPHDLy5swnpeYAMK-jWCnd2fvplsRfg130_provenance a np:Provenance .
  
  dgn-np:NP855548.RAOjoFA_EDac62xPHDLy5swnpeYAMK-jWCnd2fvplsRfg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP855548.RAOjoFA_EDac62xPHDLy5swnpeYAMK-jWCnd2fvplsRfg130_assertion {
  miriam-gene:5554 a ncit:C16612 .
  
  lld:C0151942 a ncit:C7057 .
  
  dgn-gda:DGN284a17482bd22fbefd5064bbf3734604 sio:SIO_000628 miriam-gene:5554, lld:C0151942;
    a sio:SIO_001121 .
}

dgn-np:NP855548.RAOjoFA_EDac62xPHDLy5swnpeYAMK-jWCnd2fvplsRfg130_provenance {
  dgn-np:NP855548.RAOjoFA_EDac62xPHDLy5swnpeYAMK-jWCnd2fvplsRfg130_assertion dcterms:description
      "[Risks for venous thromboembolism in genetically affected persons are substantially higher among patients with coexistent predispositions for thrombosis, such as advanced age, use of oral contraceptives, hyperhomocystinemia, and deficiencies of protein C and protein S. Factor V Leiden mutation does not seem to increase risks for arterial thrombosis.]. 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:9382368;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP855548.RAOjoFA_EDac62xPHDLy5swnpeYAMK-jWCnd2fvplsRfg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:43+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" .
}