@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP259444.RAtuGE_7WDnriX6R_HrOaSoqLSnned1GfZrGsZ3-t2-Io> .
@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:NP259444.RAtuGE_7WDnriX6R_HrOaSoqLSnned1GfZrGsZ3-t2-Io130_head {
  this: np:hasAssertion dgn-np:NP259444.RAtuGE_7WDnriX6R_HrOaSoqLSnned1GfZrGsZ3-t2-Io130_assertion;
    np:hasProvenance dgn-np:NP259444.RAtuGE_7WDnriX6R_HrOaSoqLSnned1GfZrGsZ3-t2-Io130_provenance;
    np:hasPublicationInfo dgn-np:NP259444.RAtuGE_7WDnriX6R_HrOaSoqLSnned1GfZrGsZ3-t2-Io130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP259444.RAtuGE_7WDnriX6R_HrOaSoqLSnned1GfZrGsZ3-t2-Io130_assertion a np:Assertion .
  
  dgn-np:NP259444.RAtuGE_7WDnriX6R_HrOaSoqLSnned1GfZrGsZ3-t2-Io130_provenance a np:Provenance .
  
  dgn-np:NP259444.RAtuGE_7WDnriX6R_HrOaSoqLSnned1GfZrGsZ3-t2-Io130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP259444.RAtuGE_7WDnriX6R_HrOaSoqLSnned1GfZrGsZ3-t2-Io130_assertion {
  miriam-gene:11200 a ncit:C16612 .
  
  lld:C0009402 a ncit:C7057 .
  
  dgn-gda:DGN06acbab378f35c2100e8fafd8135cbaa sio:SIO_000628 miriam-gene:11200, lld:C0009402;
    a sio:SIO_001121 .
}

dgn-np:NP259444.RAtuGE_7WDnriX6R_HrOaSoqLSnned1GfZrGsZ3-t2-Io130_provenance {
  dgn-np:NP259444.RAtuGE_7WDnriX6R_HrOaSoqLSnned1GfZrGsZ3-t2-Io130_assertion dcterms:description
      "[We utilized the Southern Sweden population-based cancer registry to identify women with double primary breast and colorectal cancer and sequenced tumor material in order to assess the contribution of the CHEK2 1100delC to the development of such metachronous tumors.]. 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:16539695;
    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:NP259444.RAtuGE_7WDnriX6R_HrOaSoqLSnned1GfZrGsZ3-t2-Io130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:25+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" .
}