@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP605451.RAIULbooeZo9gBV6m7MLVb0RriohK3ige7NZyjeBaEyhg> .
@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:NP605451.RAIULbooeZo9gBV6m7MLVb0RriohK3ige7NZyjeBaEyhg130_head {
   this: np:hasAssertion dgn-np:NP605451.RAIULbooeZo9gBV6m7MLVb0RriohK3ige7NZyjeBaEyhg130_assertion ;
    np:hasProvenance dgn-np:NP605451.RAIULbooeZo9gBV6m7MLVb0RriohK3ige7NZyjeBaEyhg130_provenance ;
    np:hasPublicationInfo dgn-np:NP605451.RAIULbooeZo9gBV6m7MLVb0RriohK3ige7NZyjeBaEyhg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP605451.RAIULbooeZo9gBV6m7MLVb0RriohK3ige7NZyjeBaEyhg130_assertion a np:Assertion .
  dgn-np:NP605451.RAIULbooeZo9gBV6m7MLVb0RriohK3ige7NZyjeBaEyhg130_provenance a np:Provenance .
  dgn-np:NP605451.RAIULbooeZo9gBV6m7MLVb0RriohK3ige7NZyjeBaEyhg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP605451.RAIULbooeZo9gBV6m7MLVb0RriohK3ige7NZyjeBaEyhg130_assertion {
   miriam-gene:6423 a ncit:C16612 .
  lld:C0009402 a ncit:C7057 .
  dgn-gda:DGNbb2fc726f1364f8e95550ec99770af0b sio:SIO_000628 miriam-gene:6423 , lld:C0009402 ;
    a sio:SIO_001121 .
}
dgn-np:NP605451.RAIULbooeZo9gBV6m7MLVb0RriohK3ige7NZyjeBaEyhg130_provenance {
   dgn-np:NP605451.RAIULbooeZo9gBV6m7MLVb0RriohK3ige7NZyjeBaEyhg130_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:NP605451.RAIULbooeZo9gBV6m7MLVb0RriohK3ige7NZyjeBaEyhg130_publicationInfo {
   this: dcterms:created "2014-10-02T12:38:03+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" .
}