@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP483079.RAt9qErLqiuLRG7p8k7Gt1erGptQQJ6eAkXN4mp3RpRIs> .
@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:NP483079.RAt9qErLqiuLRG7p8k7Gt1erGptQQJ6eAkXN4mp3RpRIs130_head {
  this: np:hasAssertion dgn-np:NP483079.RAt9qErLqiuLRG7p8k7Gt1erGptQQJ6eAkXN4mp3RpRIs130_assertion;
    np:hasProvenance dgn-np:NP483079.RAt9qErLqiuLRG7p8k7Gt1erGptQQJ6eAkXN4mp3RpRIs130_provenance;
    np:hasPublicationInfo dgn-np:NP483079.RAt9qErLqiuLRG7p8k7Gt1erGptQQJ6eAkXN4mp3RpRIs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP483079.RAt9qErLqiuLRG7p8k7Gt1erGptQQJ6eAkXN4mp3RpRIs130_assertion a np:Assertion .
  
  dgn-np:NP483079.RAt9qErLqiuLRG7p8k7Gt1erGptQQJ6eAkXN4mp3RpRIs130_provenance a np:Provenance .
  
  dgn-np:NP483079.RAt9qErLqiuLRG7p8k7Gt1erGptQQJ6eAkXN4mp3RpRIs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP483079.RAt9qErLqiuLRG7p8k7Gt1erGptQQJ6eAkXN4mp3RpRIs130_assertion {
  miriam-gene:9495 a ncit:C16612 .
  
  lld:C0019061 a ncit:C7057 .
  
  dgn-gda:DGN8e1bccdfc2801f6edd598a8fe4fc9872 sio:SIO_000628 miriam-gene:9495, lld:C0019061;
    a sio:SIO_001121 .
}

dgn-np:NP483079.RAt9qErLqiuLRG7p8k7Gt1erGptQQJ6eAkXN4mp3RpRIs130_provenance {
  dgn-np:NP483079.RAt9qErLqiuLRG7p8k7Gt1erGptQQJ6eAkXN4mp3RpRIs130_assertion dcterms:description
      "[In conclusion, potentially pathogenic O113:H21 STEC isolates carrying virulence markers in common with O113:H21 clones associated with haemolytic uraemic syndrome cases in other regions were demonstrated to occur in the natural reservoir in our settings, and therefore the risk represented by them to public health should be carefully monitored.]. 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:20223897;
    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:NP483079.RAt9qErLqiuLRG7p8k7Gt1erGptQQJ6eAkXN4mp3RpRIs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:49+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" .
}