@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP47301.RAheABmHiZszHFI_hZzySce7YH8tUJwTErSJmoTltLzTI> .
@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 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:NP47301.RAheABmHiZszHFI_hZzySce7YH8tUJwTErSJmoTltLzTI130_head {
  this: np:hasAssertion dgn-np:NP47301.RAheABmHiZszHFI_hZzySce7YH8tUJwTErSJmoTltLzTI130_assertion;
    np:hasProvenance dgn-np:NP47301.RAheABmHiZszHFI_hZzySce7YH8tUJwTErSJmoTltLzTI130_provenance;
    np:hasPublicationInfo dgn-np:NP47301.RAheABmHiZszHFI_hZzySce7YH8tUJwTErSJmoTltLzTI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP47301.RAheABmHiZszHFI_hZzySce7YH8tUJwTErSJmoTltLzTI130_assertion a np:Assertion .
  
  dgn-np:NP47301.RAheABmHiZszHFI_hZzySce7YH8tUJwTErSJmoTltLzTI130_provenance a np:Provenance .
  
  dgn-np:NP47301.RAheABmHiZszHFI_hZzySce7YH8tUJwTErSJmoTltLzTI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP47301.RAheABmHiZszHFI_hZzySce7YH8tUJwTErSJmoTltLzTI130_assertion {
  miriam-gene:595 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
  dgn-gda:DGN04a5139f22fd2db4c206575b92f96298 sio:SIO_000628 miriam-gene:595, lld:C1527249;
    a sio:SIO_001122 .
}

dgn-np:NP47301.RAheABmHiZszHFI_hZzySce7YH8tUJwTErSJmoTltLzTI130_provenance {
  dgn-np:NP47301.RAheABmHiZszHFI_hZzySce7YH8tUJwTErSJmoTltLzTI130_assertion dct:description
      "[Polymorphisms in the 2 cell-cycle control genes Aurora A and Cyclin D1 have previously been associated with changes in the age of onset of colorectal cancer in persons harboring germline mutations in DNA mismatch repair genes associated with hereditary nonpolyposis colorectal cancer (HNPCC).]. 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:18027856;
    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:NP47301.RAheABmHiZszHFI_hZzySce7YH8tUJwTErSJmoTltLzTI130_publicationInfo {
  this: dct:created "2014-10-02T12:32:21+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}