@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP47305.RAzwu5VJDfYAc-LzH1HGfxzi1smrt2Ofur1iqY8VB4SHk> .
@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:NP47305.RAzwu5VJDfYAc-LzH1HGfxzi1smrt2Ofur1iqY8VB4SHk130_head {
  this: np:hasAssertion dgn-np:NP47305.RAzwu5VJDfYAc-LzH1HGfxzi1smrt2Ofur1iqY8VB4SHk130_assertion;
    np:hasProvenance dgn-np:NP47305.RAzwu5VJDfYAc-LzH1HGfxzi1smrt2Ofur1iqY8VB4SHk130_provenance;
    np:hasPublicationInfo dgn-np:NP47305.RAzwu5VJDfYAc-LzH1HGfxzi1smrt2Ofur1iqY8VB4SHk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP47305.RAzwu5VJDfYAc-LzH1HGfxzi1smrt2Ofur1iqY8VB4SHk130_assertion a np:Assertion .
  
  dgn-np:NP47305.RAzwu5VJDfYAc-LzH1HGfxzi1smrt2Ofur1iqY8VB4SHk130_provenance a np:Provenance .
  
  dgn-np:NP47305.RAzwu5VJDfYAc-LzH1HGfxzi1smrt2Ofur1iqY8VB4SHk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP47305.RAzwu5VJDfYAc-LzH1HGfxzi1smrt2Ofur1iqY8VB4SHk130_assertion {
  miriam-gene:595 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
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    a sio:SIO_001122 .
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dgn-np:NP47305.RAzwu5VJDfYAc-LzH1HGfxzi1smrt2Ofur1iqY8VB4SHk130_provenance {
  dgn-np:NP47305.RAzwu5VJDfYAc-LzH1HGfxzi1smrt2Ofur1iqY8VB4SHk130_assertion dcterms:description
      "[We analysed 181 colorectal cancer cases and 475 matched controls and 524 adenoma cases and 517 matched controls within women in the Nurses' Health Study (NHS) cohort, 171 colorectal cancer cases and 347 matched controls and 372 adenoma cases and 712 matched controls nested within men in the Health Professionals' Follow-Up Study (HPFS) cohort, and 258 colorectal cancer cases and 415 matched controls within men in the Physicians' Health Study (PHS) cohort to assess the risk associated with the CCND1 A870G genotype.]. 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:16495921;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP47305.RAzwu5VJDfYAc-LzH1HGfxzi1smrt2Ofur1iqY8VB4SHk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:21+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" .
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