@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP889549.RAdrR8cYAZTJSPn-4e4K8_3usL59Y6As2wb_AUG0hLcLs> .
@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:NP889549.RAdrR8cYAZTJSPn-4e4K8_3usL59Y6As2wb_AUG0hLcLs130_head {
  this: np:hasAssertion dgn-np:NP889549.RAdrR8cYAZTJSPn-4e4K8_3usL59Y6As2wb_AUG0hLcLs130_assertion;
    np:hasProvenance dgn-np:NP889549.RAdrR8cYAZTJSPn-4e4K8_3usL59Y6As2wb_AUG0hLcLs130_provenance;
    np:hasPublicationInfo dgn-np:NP889549.RAdrR8cYAZTJSPn-4e4K8_3usL59Y6As2wb_AUG0hLcLs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP889549.RAdrR8cYAZTJSPn-4e4K8_3usL59Y6As2wb_AUG0hLcLs130_assertion a np:Assertion .
  
  dgn-np:NP889549.RAdrR8cYAZTJSPn-4e4K8_3usL59Y6As2wb_AUG0hLcLs130_provenance a np:Provenance .
  
  dgn-np:NP889549.RAdrR8cYAZTJSPn-4e4K8_3usL59Y6As2wb_AUG0hLcLs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP889549.RAdrR8cYAZTJSPn-4e4K8_3usL59Y6As2wb_AUG0hLcLs130_assertion {
  miriam-gene:231 a ncit:C16612 .
  
  lld:C0011609 a ncit:C7057 .
  
  dgn-gda:DGNdb389b7b080d659324994b79cc05c63b sio:SIO_000628 miriam-gene:231, lld:C0011609;
    a sio:SIO_001121 .
}

dgn-np:NP889549.RAdrR8cYAZTJSPn-4e4K8_3usL59Y6As2wb_AUG0hLcLs130_provenance {
  dgn-np:NP889549.RAdrR8cYAZTJSPn-4e4K8_3usL59Y6As2wb_AUG0hLcLs130_assertion dcterms:description
      "[In the field of severe cutaneous adverse drug reactions (cutaneous ADR) such as Stevens-Johnson syndrome (SJS), toxic epidermal necrolysis (TEN), and drug-induced hypersensitivity syndrome (DHIS) or drug rash with eosinophilia and systemic symptoms (DRESS), major advances have recently been gained through studies of an association between HLA alleles and drug hypersensitivity induced by specific drugs.]. 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:21342226;
    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:NP889549.RAdrR8cYAZTJSPn-4e4K8_3usL59Y6As2wb_AUG0hLcLs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:07+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" .
}