@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP542816.RA2AVIwR56XkMoj1oQVQGF42X5mzJamkxd1sSBL6Kphg0> .
@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:NP542816.RA2AVIwR56XkMoj1oQVQGF42X5mzJamkxd1sSBL6Kphg0130_head {
  this: np:hasAssertion dgn-np:NP542816.RA2AVIwR56XkMoj1oQVQGF42X5mzJamkxd1sSBL6Kphg0130_assertion;
    np:hasProvenance dgn-np:NP542816.RA2AVIwR56XkMoj1oQVQGF42X5mzJamkxd1sSBL6Kphg0130_provenance;
    np:hasPublicationInfo dgn-np:NP542816.RA2AVIwR56XkMoj1oQVQGF42X5mzJamkxd1sSBL6Kphg0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP542816.RA2AVIwR56XkMoj1oQVQGF42X5mzJamkxd1sSBL6Kphg0130_assertion a np:Assertion .
  
  dgn-np:NP542816.RA2AVIwR56XkMoj1oQVQGF42X5mzJamkxd1sSBL6Kphg0130_provenance a np:Provenance .
  
  dgn-np:NP542816.RA2AVIwR56XkMoj1oQVQGF42X5mzJamkxd1sSBL6Kphg0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP542816.RA2AVIwR56XkMoj1oQVQGF42X5mzJamkxd1sSBL6Kphg0130_assertion {
  miriam-gene:2054 a ncit:C16612 .
  
  lld:C0019061 a ncit:C7057 .
  
  dgn-gda:DGN5be4d5de5a8fdcb10f21276933476e88 sio:SIO_000628 miriam-gene:2054, lld:C0019061;
    a sio:SIO_001121 .
}

dgn-np:NP542816.RA2AVIwR56XkMoj1oQVQGF42X5mzJamkxd1sSBL6Kphg0130_provenance {
  dgn-np:NP542816.RA2AVIwR56XkMoj1oQVQGF42X5mzJamkxd1sSBL6Kphg0130_assertion dcterms:description
      "[Whereas the presence of the STX2 or STX2C genotype is associated with the ability of STEC to cause the hemolytic uremic syndrome (HUS), strains possessing STX2D or STX2E have been isolated from patients with less severe disease.]. 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:16575685;
    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:NP542816.RA2AVIwR56XkMoj1oQVQGF42X5mzJamkxd1sSBL6Kphg0130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:51+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" .
}