@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP47579.RAkmQrLB_zP-jP-FrbYwGOPBrjgYUChN_EEW0bOcv7mGk> .
@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:NP47579.RAkmQrLB_zP-jP-FrbYwGOPBrjgYUChN_EEW0bOcv7mGk130_head {
  this: np:hasAssertion dgn-np:NP47579.RAkmQrLB_zP-jP-FrbYwGOPBrjgYUChN_EEW0bOcv7mGk130_assertion;
    np:hasProvenance dgn-np:NP47579.RAkmQrLB_zP-jP-FrbYwGOPBrjgYUChN_EEW0bOcv7mGk130_provenance;
    np:hasPublicationInfo dgn-np:NP47579.RAkmQrLB_zP-jP-FrbYwGOPBrjgYUChN_EEW0bOcv7mGk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP47579.RAkmQrLB_zP-jP-FrbYwGOPBrjgYUChN_EEW0bOcv7mGk130_assertion a np:Assertion .
  
  dgn-np:NP47579.RAkmQrLB_zP-jP-FrbYwGOPBrjgYUChN_EEW0bOcv7mGk130_provenance a np:Provenance .
  
  dgn-np:NP47579.RAkmQrLB_zP-jP-FrbYwGOPBrjgYUChN_EEW0bOcv7mGk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP47579.RAkmQrLB_zP-jP-FrbYwGOPBrjgYUChN_EEW0bOcv7mGk130_assertion {
  miriam-gene:843 a ncit:C16612 .
  
  lld:C0006142 a ncit:C7057 .
  
  dgn-gda:DGNa32da05fb06b9b814f64b0a53b35253a sio:SIO_000628 miriam-gene:843, lld:C0006142;
    a sio:SIO_001122 .
}

dgn-np:NP47579.RAkmQrLB_zP-jP-FrbYwGOPBrjgYUChN_EEW0bOcv7mGk130_provenance {
  dgn-np:NP47579.RAkmQrLB_zP-jP-FrbYwGOPBrjgYUChN_EEW0bOcv7mGk130_assertion dct:description
      "[our data provide persuasive evidence against an overall association between invasive breast cancer risk and ERCC4 rs744154, TNF rs361525, CASP10 rs13010627, PGR rs1042838, and BID rs8190315 genotypes among women of European descent.]. 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:19423537;
    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:NP47579.RAkmQrLB_zP-jP-FrbYwGOPBrjgYUChN_EEW0bOcv7mGk130_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" .
}