@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP219674.RAFkkO0iCa9k7ThxF6Xmv8Ep2tg10CpZYXnSnm3Vu6eAA> .
@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:NP219674.RAFkkO0iCa9k7ThxF6Xmv8Ep2tg10CpZYXnSnm3Vu6eAA130_head {
  this: np:hasAssertion dgn-np:NP219674.RAFkkO0iCa9k7ThxF6Xmv8Ep2tg10CpZYXnSnm3Vu6eAA130_assertion;
    np:hasProvenance dgn-np:NP219674.RAFkkO0iCa9k7ThxF6Xmv8Ep2tg10CpZYXnSnm3Vu6eAA130_provenance;
    np:hasPublicationInfo dgn-np:NP219674.RAFkkO0iCa9k7ThxF6Xmv8Ep2tg10CpZYXnSnm3Vu6eAA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP219674.RAFkkO0iCa9k7ThxF6Xmv8Ep2tg10CpZYXnSnm3Vu6eAA130_assertion a np:Assertion .
  
  dgn-np:NP219674.RAFkkO0iCa9k7ThxF6Xmv8Ep2tg10CpZYXnSnm3Vu6eAA130_provenance a np:Provenance .
  
  dgn-np:NP219674.RAFkkO0iCa9k7ThxF6Xmv8Ep2tg10CpZYXnSnm3Vu6eAA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP219674.RAFkkO0iCa9k7ThxF6Xmv8Ep2tg10CpZYXnSnm3Vu6eAA130_assertion {
  miriam-gene:3565 a ncit:C16612 .
  
  lld:C0153381 a ncit:C7057 .
  
  dgn-gda:DGN22d1c14ff6e25ecf863b5bea6a40e003 sio:SIO_000628 miriam-gene:3565, lld:C0153381;
    a sio:SIO_001121 .
}

dgn-np:NP219674.RAFkkO0iCa9k7ThxF6Xmv8Ep2tg10CpZYXnSnm3Vu6eAA130_provenance {
  dgn-np:NP219674.RAFkkO0iCa9k7ThxF6Xmv8Ep2tg10CpZYXnSnm3Vu6eAA130_assertion dcterms:description
      "[Taken together, our results indicated that IL-4 rs2243250 polymorphism was associated with decreased oral cancer risk in both the homozygote contrasts and the dominant genetic model, as well as increased renal cell cancer risk in both the homozygote contrasts and the recessive genetic model.]. 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:23572437;
    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:NP219674.RAFkkO0iCa9k7ThxF6Xmv8Ep2tg10CpZYXnSnm3Vu6eAA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:02+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" .
}