@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP400901.RABWcWfQE95y-pR7gwZk490hyUD7ymnt91FgsutCxJTgQ> .
@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:NP400901.RABWcWfQE95y-pR7gwZk490hyUD7ymnt91FgsutCxJTgQ130_head {
  this: np:hasAssertion dgn-np:NP400901.RABWcWfQE95y-pR7gwZk490hyUD7ymnt91FgsutCxJTgQ130_assertion;
    np:hasProvenance dgn-np:NP400901.RABWcWfQE95y-pR7gwZk490hyUD7ymnt91FgsutCxJTgQ130_provenance;
    np:hasPublicationInfo dgn-np:NP400901.RABWcWfQE95y-pR7gwZk490hyUD7ymnt91FgsutCxJTgQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP400901.RABWcWfQE95y-pR7gwZk490hyUD7ymnt91FgsutCxJTgQ130_assertion a np:Assertion .
  
  dgn-np:NP400901.RABWcWfQE95y-pR7gwZk490hyUD7ymnt91FgsutCxJTgQ130_provenance a np:Provenance .
  
  dgn-np:NP400901.RABWcWfQE95y-pR7gwZk490hyUD7ymnt91FgsutCxJTgQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP400901.RABWcWfQE95y-pR7gwZk490hyUD7ymnt91FgsutCxJTgQ130_assertion {
  miriam-gene:391110 a ncit:C16612 .
  
  lld:C0016522 a ncit:C7057 .
  
  dgn-gda:DGN928d7961fea111a7f46d01e912a30ad3 sio:SIO_000628 miriam-gene:391110, lld:C0016522;
    a sio:SIO_001121 .
}

dgn-np:NP400901.RABWcWfQE95y-pR7gwZk490hyUD7ymnt91FgsutCxJTgQ130_provenance {
  dgn-np:NP400901.RABWcWfQE95y-pR7gwZk490hyUD7ymnt91FgsutCxJTgQ130_assertion dcterms:description
      "[Further trends towards higher frequencies of the FVL mutation were found in patients with patent foramen ovale (OR 1.9), individual (OR 2.1) or family history of previous thrombembolisms (OR 2.0), and in those aged 25 years at onset of disease (OR 1.9, all not significant).]. 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:9776464;
    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:NP400901.RABWcWfQE95y-pR7gwZk490hyUD7ymnt91FgsutCxJTgQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:58+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" .
}