@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP893083.RAlQjaWemfy-Jr8U_AWZTvHCb4bsQjQsGTxCVEMknfylM> .
@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:NP893083.RAlQjaWemfy-Jr8U_AWZTvHCb4bsQjQsGTxCVEMknfylM130_head {
  this: np:hasAssertion dgn-np:NP893083.RAlQjaWemfy-Jr8U_AWZTvHCb4bsQjQsGTxCVEMknfylM130_assertion;
    np:hasProvenance dgn-np:NP893083.RAlQjaWemfy-Jr8U_AWZTvHCb4bsQjQsGTxCVEMknfylM130_provenance;
    np:hasPublicationInfo dgn-np:NP893083.RAlQjaWemfy-Jr8U_AWZTvHCb4bsQjQsGTxCVEMknfylM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP893083.RAlQjaWemfy-Jr8U_AWZTvHCb4bsQjQsGTxCVEMknfylM130_assertion a np:Assertion .
  
  dgn-np:NP893083.RAlQjaWemfy-Jr8U_AWZTvHCb4bsQjQsGTxCVEMknfylM130_provenance a np:Provenance .
  
  dgn-np:NP893083.RAlQjaWemfy-Jr8U_AWZTvHCb4bsQjQsGTxCVEMknfylM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP893083.RAlQjaWemfy-Jr8U_AWZTvHCb4bsQjQsGTxCVEMknfylM130_assertion {
  miriam-gene:2153 a ncit:C16612 .
  
  lld:C0007785 a ncit:C7057 .
  
  dgn-gda:DGNc90e90887f1c4a59d97f1eea2d692a7e sio:SIO_000628 miriam-gene:2153, lld:C0007785;
    a sio:SIO_001121 .
}

dgn-np:NP893083.RAlQjaWemfy-Jr8U_AWZTvHCb4bsQjQsGTxCVEMknfylM130_provenance {
  dgn-np:NP893083.RAlQjaWemfy-Jr8U_AWZTvHCb4bsQjQsGTxCVEMknfylM130_assertion dcterms:description
      "[We examined FVL and PT G20210A mutation in 220 patients (group 1) with cerebral ischemia associated with a PFO and without other etiology, in 196 patients with cerebral ischemia of an etiology other than PFO (group 2), and in 362 healthy subjects (group 3) from the same region in Germany.]. 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:12766367;
    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:NP893083.RAlQjaWemfy-Jr8U_AWZTvHCb4bsQjQsGTxCVEMknfylM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:09+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" .
}