@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP165277.RAclHqIzO92TSmzNYxlAroDJZTLHM6SDkTQvkgS1X1wlI> .
@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:NP165277.RAclHqIzO92TSmzNYxlAroDJZTLHM6SDkTQvkgS1X1wlI130_head {
  this: np:hasAssertion dgn-np:NP165277.RAclHqIzO92TSmzNYxlAroDJZTLHM6SDkTQvkgS1X1wlI130_assertion;
    np:hasProvenance dgn-np:NP165277.RAclHqIzO92TSmzNYxlAroDJZTLHM6SDkTQvkgS1X1wlI130_provenance;
    np:hasPublicationInfo dgn-np:NP165277.RAclHqIzO92TSmzNYxlAroDJZTLHM6SDkTQvkgS1X1wlI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP165277.RAclHqIzO92TSmzNYxlAroDJZTLHM6SDkTQvkgS1X1wlI130_assertion a np:Assertion .
  
  dgn-np:NP165277.RAclHqIzO92TSmzNYxlAroDJZTLHM6SDkTQvkgS1X1wlI130_provenance a np:Provenance .
  
  dgn-np:NP165277.RAclHqIzO92TSmzNYxlAroDJZTLHM6SDkTQvkgS1X1wlI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP165277.RAclHqIzO92TSmzNYxlAroDJZTLHM6SDkTQvkgS1X1wlI130_assertion {
  miriam-gene:8840 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
  dgn-gda:DGNf73582669a155b81889e282b8c4499b8 sio:SIO_000628 miriam-gene:8840, lld:C1527249;
    a sio:SIO_001121 .
}

dgn-np:NP165277.RAclHqIzO92TSmzNYxlAroDJZTLHM6SDkTQvkgS1X1wlI130_provenance {
  dgn-np:NP165277.RAclHqIzO92TSmzNYxlAroDJZTLHM6SDkTQvkgS1X1wlI130_assertion dcterms:description
      "[This population-based case-control study, including 1795 CRC cases and 1805 controls, investigates the association between common, putative functional polymorphisms in DNFA5, HIF1A, NDRG1, PYGO1, SFRP2, SFRP4, WISP1 and WISP3 genes and CRC risk.]. 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:20403915;
    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:NP165277.RAclHqIzO92TSmzNYxlAroDJZTLHM6SDkTQvkgS1X1wlI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:29+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" .
}