@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP223545.RAfLBc109pGDWY_LD7DQkfqctBho35UE6q4uI0iclqtOU> .
@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:NP223545.RAfLBc109pGDWY_LD7DQkfqctBho35UE6q4uI0iclqtOU130_head {
   this: np:hasAssertion dgn-np:NP223545.RAfLBc109pGDWY_LD7DQkfqctBho35UE6q4uI0iclqtOU130_assertion ;
    np:hasProvenance dgn-np:NP223545.RAfLBc109pGDWY_LD7DQkfqctBho35UE6q4uI0iclqtOU130_provenance ;
    np:hasPublicationInfo dgn-np:NP223545.RAfLBc109pGDWY_LD7DQkfqctBho35UE6q4uI0iclqtOU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP223545.RAfLBc109pGDWY_LD7DQkfqctBho35UE6q4uI0iclqtOU130_assertion a np:Assertion .
  dgn-np:NP223545.RAfLBc109pGDWY_LD7DQkfqctBho35UE6q4uI0iclqtOU130_provenance a np:Provenance .
  dgn-np:NP223545.RAfLBc109pGDWY_LD7DQkfqctBho35UE6q4uI0iclqtOU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP223545.RAfLBc109pGDWY_LD7DQkfqctBho35UE6q4uI0iclqtOU130_assertion {
   miriam-gene:26108 a ncit:C16612 .
  lld:C1527249 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP223545.RAfLBc109pGDWY_LD7DQkfqctBho35UE6q4uI0iclqtOU130_provenance {
   dgn-np:NP223545.RAfLBc109pGDWY_LD7DQkfqctBho35UE6q4uI0iclqtOU130_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 ;
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    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 ;
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}
dgn-np:NP223545.RAfLBc109pGDWY_LD7DQkfqctBho35UE6q4uI0iclqtOU130_publicationInfo {
   this: dcterms:created "2014-10-02T12:34:04+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 ;
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}