@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP201209.RAUEYHi70AEwkDjx0nnzKBgSwo38Sx6JmUEHXW8BwxjFY> .
@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:NP201209.RAUEYHi70AEwkDjx0nnzKBgSwo38Sx6JmUEHXW8BwxjFY130_head {
  this: np:hasAssertion dgn-np:NP201209.RAUEYHi70AEwkDjx0nnzKBgSwo38Sx6JmUEHXW8BwxjFY130_assertion;
    np:hasProvenance dgn-np:NP201209.RAUEYHi70AEwkDjx0nnzKBgSwo38Sx6JmUEHXW8BwxjFY130_provenance;
    np:hasPublicationInfo dgn-np:NP201209.RAUEYHi70AEwkDjx0nnzKBgSwo38Sx6JmUEHXW8BwxjFY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP201209.RAUEYHi70AEwkDjx0nnzKBgSwo38Sx6JmUEHXW8BwxjFY130_assertion a np:Assertion .
  
  dgn-np:NP201209.RAUEYHi70AEwkDjx0nnzKBgSwo38Sx6JmUEHXW8BwxjFY130_provenance a np:Provenance .
  
  dgn-np:NP201209.RAUEYHi70AEwkDjx0nnzKBgSwo38Sx6JmUEHXW8BwxjFY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP201209.RAUEYHi70AEwkDjx0nnzKBgSwo38Sx6JmUEHXW8BwxjFY130_assertion {
  miriam-gene:149233 a ncit:C16612 .
  
  lld:C0596263 a ncit:C7057 .
  
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    a sio:SIO_001121 .
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dgn-np:NP201209.RAUEYHi70AEwkDjx0nnzKBgSwo38Sx6JmUEHXW8BwxjFY130_provenance {
  dgn-np:NP201209.RAUEYHi70AEwkDjx0nnzKBgSwo38Sx6JmUEHXW8BwxjFY130_assertion dcterms:description
      "[In this comprehensive study of genetic variability in IL23R across the spectrum of colorectal carcinogenesis, as well as within colon and rectal tumor molecular subtypes, we observed associations between SNPs in IL23R and risk of rectal cancer: the 88413 C>A (rs10889675) and 69450 C>A (rs7542081) polymorphisms were associated with decreased rectal cancer risk overall (p-trend=0.04 and 0.05 respectively), and specifically with rectal tumors bearing a TP53 mutation (88413 CA/AA vs. CC OR: 0.66; 95% CI: 0.46-94; 69450 CA/AA vs. CC OR: 0.60; 95% CI: 0.37-0.98).]. 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:22154103;
    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:NP201209.RAUEYHi70AEwkDjx0nnzKBgSwo38Sx6JmUEHXW8BwxjFY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:51+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: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>;
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