@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP78642.RA5tNK3CvSG61XEZCkQiqlQIuLLF-dgi-H5du775tgRYk> .
@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:NP78642.RA5tNK3CvSG61XEZCkQiqlQIuLLF-dgi-H5du775tgRYk130_head {
  this: np:hasAssertion dgn-np:NP78642.RA5tNK3CvSG61XEZCkQiqlQIuLLF-dgi-H5du775tgRYk130_assertion;
    np:hasProvenance dgn-np:NP78642.RA5tNK3CvSG61XEZCkQiqlQIuLLF-dgi-H5du775tgRYk130_provenance;
    np:hasPublicationInfo dgn-np:NP78642.RA5tNK3CvSG61XEZCkQiqlQIuLLF-dgi-H5du775tgRYk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP78642.RA5tNK3CvSG61XEZCkQiqlQIuLLF-dgi-H5du775tgRYk130_assertion a np:Assertion .
  
  dgn-np:NP78642.RA5tNK3CvSG61XEZCkQiqlQIuLLF-dgi-H5du775tgRYk130_provenance a np:Provenance .
  
  dgn-np:NP78642.RA5tNK3CvSG61XEZCkQiqlQIuLLF-dgi-H5du775tgRYk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP78642.RA5tNK3CvSG61XEZCkQiqlQIuLLF-dgi-H5du775tgRYk130_assertion {
  miriam-gene:51174 a ncit:C16612 .
  
  lld:C0006142 a ncit:C7057 .
  
  dgn-gda:DGN01ff057076b4d1b459b12bd53c0484e3 sio:SIO_000628 miriam-gene:51174, lld:C0006142;
    a sio:SIO_001122 .
}

dgn-np:NP78642.RA5tNK3CvSG61XEZCkQiqlQIuLLF-dgi-H5du775tgRYk130_provenance {
  dgn-np:NP78642.RA5tNK3CvSG61XEZCkQiqlQIuLLF-dgi-H5du775tgRYk130_assertion dct:description
      "[These findings suggest that single polymorphisms and combinations of polymorphisms within candidate oncogenes from the 17q23 amplicon may influence risk of breast cancer overall and possibly specific molecular subtypes of breast 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:19454617;
    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:NP78642.RA5tNK3CvSG61XEZCkQiqlQIuLLF-dgi-H5du775tgRYk130_publicationInfo {
  this: dct:created "2014-10-02T12:32:38+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" .
}