@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP641356.RAtLjnQyFkjUSC0obEZloJ8G6KTGLFIqh6VwwlwsxMGr0> .
@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/v3.0.0/void/> .

dgn-np:NP641356.RAtLjnQyFkjUSC0obEZloJ8G6KTGLFIqh6VwwlwsxMGr0130_head {
  this: np:hasAssertion dgn-np:NP641356.RAtLjnQyFkjUSC0obEZloJ8G6KTGLFIqh6VwwlwsxMGr0130_assertion;
    np:hasProvenance dgn-np:NP641356.RAtLjnQyFkjUSC0obEZloJ8G6KTGLFIqh6VwwlwsxMGr0130_provenance;
    np:hasPublicationInfo dgn-np:NP641356.RAtLjnQyFkjUSC0obEZloJ8G6KTGLFIqh6VwwlwsxMGr0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP641356.RAtLjnQyFkjUSC0obEZloJ8G6KTGLFIqh6VwwlwsxMGr0130_assertion a np:Assertion .
  
  dgn-np:NP641356.RAtLjnQyFkjUSC0obEZloJ8G6KTGLFIqh6VwwlwsxMGr0130_provenance a np:Provenance .
  
  dgn-np:NP641356.RAtLjnQyFkjUSC0obEZloJ8G6KTGLFIqh6VwwlwsxMGr0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP641356.RAtLjnQyFkjUSC0obEZloJ8G6KTGLFIqh6VwwlwsxMGr0130_assertion {
  miriam-gene:5555 a ncit:C16612 .
  
  lld:C0151942 a ncit:C7057 .
  
  dgn-gda:DGN1f88d54ae275cdbe6f254cd1f4ee65b4 sio:SIO_000628 miriam-gene:5555, lld:C0151942;
    a sio:SIO_001121 .
}

dgn-np:NP641356.RAtLjnQyFkjUSC0obEZloJ8G6KTGLFIqh6VwwlwsxMGr0130_provenance {
  dgn-np:NP641356.RAtLjnQyFkjUSC0obEZloJ8G6KTGLFIqh6VwwlwsxMGr0130_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-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP641356.RAtLjnQyFkjUSC0obEZloJ8G6KTGLFIqh6VwwlwsxMGr0130_publicationInfo {
  this: dcterms:created "2015-08-25T14:44:04+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}