@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1386592.RAcHrAhD8BhyH9rKBxwE4M5A9sZQQIeIGHdHeLuevAIag> .
@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:NP1386592.RAcHrAhD8BhyH9rKBxwE4M5A9sZQQIeIGHdHeLuevAIag130_head {
  this: np:hasAssertion dgn-np:NP1386592.RAcHrAhD8BhyH9rKBxwE4M5A9sZQQIeIGHdHeLuevAIag130_assertion;
    np:hasProvenance dgn-np:NP1386592.RAcHrAhD8BhyH9rKBxwE4M5A9sZQQIeIGHdHeLuevAIag130_provenance;
    np:hasPublicationInfo dgn-np:NP1386592.RAcHrAhD8BhyH9rKBxwE4M5A9sZQQIeIGHdHeLuevAIag130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1386592.RAcHrAhD8BhyH9rKBxwE4M5A9sZQQIeIGHdHeLuevAIag130_assertion a np:Assertion .
  
  dgn-np:NP1386592.RAcHrAhD8BhyH9rKBxwE4M5A9sZQQIeIGHdHeLuevAIag130_provenance a np:Provenance .
  
  dgn-np:NP1386592.RAcHrAhD8BhyH9rKBxwE4M5A9sZQQIeIGHdHeLuevAIag130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1386592.RAcHrAhD8BhyH9rKBxwE4M5A9sZQQIeIGHdHeLuevAIag130_assertion {
  miriam-gene:2147 a ncit:C16612 .
  
  lld:C0040038 a ncit:C7057 .
  
  dgn-gda:DGNae4267b792aa174991a82326f7200fcc sio:SIO_000628 miriam-gene:2147, lld:C0040038;
    a sio:SIO_001121 .
}

dgn-np:NP1386592.RAcHrAhD8BhyH9rKBxwE4M5A9sZQQIeIGHdHeLuevAIag130_provenance {
  dgn-np:NP1386592.RAcHrAhD8BhyH9rKBxwE4M5A9sZQQIeIGHdHeLuevAIag130_assertion dcterms:description
      "[We have demonstrated that the prevalence of the PT 20210A allele is significantly greater in subjects with venous thrombosis and characterised heritable thrombophilia than in normal control subjects and that the additional inheritance of PT 20210A is associated with an increased risk of venous thromboembolism.]. 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:9423788;
    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:NP1386592.RAcHrAhD8BhyH9rKBxwE4M5A9sZQQIeIGHdHeLuevAIag130_publicationInfo {
  this: dcterms:created "2016-05-13T12:52:14+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" .
}