@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP496071.RAeWFdP1GxJfiNuMtT_wmAkYwdW2uFP5xOzspBDXNCY-c> .
@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/v3.0.0/void/> .

dgn-np:NP496071.RAeWFdP1GxJfiNuMtT_wmAkYwdW2uFP5xOzspBDXNCY-c130_head {
  this: np:hasAssertion dgn-np:NP496071.RAeWFdP1GxJfiNuMtT_wmAkYwdW2uFP5xOzspBDXNCY-c130_assertion;
    np:hasProvenance dgn-np:NP496071.RAeWFdP1GxJfiNuMtT_wmAkYwdW2uFP5xOzspBDXNCY-c130_provenance;
    np:hasPublicationInfo dgn-np:NP496071.RAeWFdP1GxJfiNuMtT_wmAkYwdW2uFP5xOzspBDXNCY-c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP496071.RAeWFdP1GxJfiNuMtT_wmAkYwdW2uFP5xOzspBDXNCY-c130_assertion a np:Assertion .
  
  dgn-np:NP496071.RAeWFdP1GxJfiNuMtT_wmAkYwdW2uFP5xOzspBDXNCY-c130_provenance a np:Provenance .
  
  dgn-np:NP496071.RAeWFdP1GxJfiNuMtT_wmAkYwdW2uFP5xOzspBDXNCY-c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP496071.RAeWFdP1GxJfiNuMtT_wmAkYwdW2uFP5xOzspBDXNCY-c130_assertion {
  miriam-gene:3566 a ncit:C16612 .
  
  lld:C3539909 a ncit:C7057 .
  
  dgn-gda:DGN11ebb6b34081c27496160124f10ed93b sio:SIO_000628 miriam-gene:3566, lld:C3539909;
    a sio:SIO_001122 .
}

dgn-np:NP496071.RAeWFdP1GxJfiNuMtT_wmAkYwdW2uFP5xOzspBDXNCY-c130_provenance {
  dgn-np:NP496071.RAeWFdP1GxJfiNuMtT_wmAkYwdW2uFP5xOzspBDXNCY-c130_assertion dcterms:description
      "[The combination of the less frequent allele of the IL13 R130Q polymorphism with any of the predominant homozygous genotypes of the three polymorphisms of IL4RA was more significantly associated with the risk of betalactam allergy (P=0.0006, 0.0077, and 0.0041, respectively) than any polymorphism considered alone (P=0.1745, 0.0268, 0.1812, 0.0152, respectively).]. 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:17001290;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP496071.RAeWFdP1GxJfiNuMtT_wmAkYwdW2uFP5xOzspBDXNCY-c130_publicationInfo {
  this: dcterms:created "2015-08-25T14:42:33+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}