@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP56431.RAsvmY42RUkDoEhzDopcShLoPJwja2mZ2ct3KbtVLkU7I> .
@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:NP56431.RAsvmY42RUkDoEhzDopcShLoPJwja2mZ2ct3KbtVLkU7I130_head {
  this: np:hasAssertion dgn-np:NP56431.RAsvmY42RUkDoEhzDopcShLoPJwja2mZ2ct3KbtVLkU7I130_assertion;
    np:hasProvenance dgn-np:NP56431.RAsvmY42RUkDoEhzDopcShLoPJwja2mZ2ct3KbtVLkU7I130_provenance;
    np:hasPublicationInfo dgn-np:NP56431.RAsvmY42RUkDoEhzDopcShLoPJwja2mZ2ct3KbtVLkU7I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP56431.RAsvmY42RUkDoEhzDopcShLoPJwja2mZ2ct3KbtVLkU7I130_assertion a np:Assertion .
  
  dgn-np:NP56431.RAsvmY42RUkDoEhzDopcShLoPJwja2mZ2ct3KbtVLkU7I130_provenance a np:Provenance .
  
  dgn-np:NP56431.RAsvmY42RUkDoEhzDopcShLoPJwja2mZ2ct3KbtVLkU7I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP56431.RAsvmY42RUkDoEhzDopcShLoPJwja2mZ2ct3KbtVLkU7I130_assertion {
  miriam-gene:3553 a ncit:C16612 .
  
  lld:C0003615 a ncit:C7057 .
  
  dgn-gda:DGN614c19e5aba3707be9799c0401f318e6 sio:SIO_000628 miriam-gene:3553, lld:C0003615;
    a sio:SIO_001122 .
}

dgn-np:NP56431.RAsvmY42RUkDoEhzDopcShLoPJwja2mZ2ct3KbtVLkU7I130_provenance {
  dgn-np:NP56431.RAsvmY42RUkDoEhzDopcShLoPJwja2mZ2ct3KbtVLkU7I130_assertion dcterms:description
      "[ Polymorphism in the IL-6 gene was associated with the severity of appendicitis, even after adjustment for duration of symptoms. The risk for developing appendiceal perforation or gangrene may be determined, in part, by variation in the IL-6 gene.]. 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:15273551;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP56431.RAsvmY42RUkDoEhzDopcShLoPJwja2mZ2ct3KbtVLkU7I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:26+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" .
}