@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP660120.RAbjgzXT2cVDEa4YETyiwUzv3jKPIU-zQK542W0iHzRkM> .
@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:NP660120.RAbjgzXT2cVDEa4YETyiwUzv3jKPIU-zQK542W0iHzRkM130_head {
  this: np:hasAssertion dgn-np:NP660120.RAbjgzXT2cVDEa4YETyiwUzv3jKPIU-zQK542W0iHzRkM130_assertion;
    np:hasProvenance dgn-np:NP660120.RAbjgzXT2cVDEa4YETyiwUzv3jKPIU-zQK542W0iHzRkM130_provenance;
    np:hasPublicationInfo dgn-np:NP660120.RAbjgzXT2cVDEa4YETyiwUzv3jKPIU-zQK542W0iHzRkM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP660120.RAbjgzXT2cVDEa4YETyiwUzv3jKPIU-zQK542W0iHzRkM130_assertion a np:Assertion .
  
  dgn-np:NP660120.RAbjgzXT2cVDEa4YETyiwUzv3jKPIU-zQK542W0iHzRkM130_provenance a np:Provenance .
  
  dgn-np:NP660120.RAbjgzXT2cVDEa4YETyiwUzv3jKPIU-zQK542W0iHzRkM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP660120.RAbjgzXT2cVDEa4YETyiwUzv3jKPIU-zQK542W0iHzRkM130_assertion {
  miriam-gene:5055 a ncit:C16612 .
  
  lld:C0149871 a ncit:C7057 .
  
  dgn-gda:DGN4930a6dc9b4dd668d63253bf3ff893be sio:SIO_000628 miriam-gene:5055, lld:C0149871;
    a sio:SIO_001121 .
}

dgn-np:NP660120.RAbjgzXT2cVDEa4YETyiwUzv3jKPIU-zQK542W0iHzRkM130_provenance {
  dgn-np:NP660120.RAbjgzXT2cVDEa4YETyiwUzv3jKPIU-zQK542W0iHzRkM130_assertion dcterms:description
      "[The aim of this study was to estimate the risk of deep venous thrombosis (DVT) caused by the polymorphisms in the TAFI gene in relation to polymorphisms of the other fibrinolytic variables such as PAI-844A>G and t-PA-7,351C>T. This study includes 130 patients with DVT and 130 age- and sex-matched healthy controls.]. 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:14651335;
    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:NP660120.RAbjgzXT2cVDEa4YETyiwUzv3jKPIU-zQK542W0iHzRkM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:39+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" .
}