@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP43174.RAjByl_7OUCNkM0PL8cUuuLJ0beXCMiMFGRWDKCUs3Z9M> .
@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:NP43174.RAjByl_7OUCNkM0PL8cUuuLJ0beXCMiMFGRWDKCUs3Z9M130_head {
  this: np:hasAssertion dgn-np:NP43174.RAjByl_7OUCNkM0PL8cUuuLJ0beXCMiMFGRWDKCUs3Z9M130_assertion;
    np:hasProvenance dgn-np:NP43174.RAjByl_7OUCNkM0PL8cUuuLJ0beXCMiMFGRWDKCUs3Z9M130_provenance;
    np:hasPublicationInfo dgn-np:NP43174.RAjByl_7OUCNkM0PL8cUuuLJ0beXCMiMFGRWDKCUs3Z9M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP43174.RAjByl_7OUCNkM0PL8cUuuLJ0beXCMiMFGRWDKCUs3Z9M130_assertion a np:Assertion .
  
  dgn-np:NP43174.RAjByl_7OUCNkM0PL8cUuuLJ0beXCMiMFGRWDKCUs3Z9M130_provenance a np:Provenance .
  
  dgn-np:NP43174.RAjByl_7OUCNkM0PL8cUuuLJ0beXCMiMFGRWDKCUs3Z9M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP43174.RAjByl_7OUCNkM0PL8cUuuLJ0beXCMiMFGRWDKCUs3Z9M130_assertion {
  miriam-gene:2944 a ncit:C16612 .
  
  lld:C0006142 a ncit:C7057 .
  
  dgn-gda:DGN384f3c1d5d42263f0f8ca4d7c3663bc3 sio:SIO_000628 miriam-gene:2944, lld:C0006142;
    a sio:SIO_001122 .
}

dgn-np:NP43174.RAjByl_7OUCNkM0PL8cUuuLJ0beXCMiMFGRWDKCUs3Z9M130_provenance {
  dgn-np:NP43174.RAjByl_7OUCNkM0PL8cUuuLJ0beXCMiMFGRWDKCUs3Z9M130_assertion dct:description
      "[To evaluate the occurrence of homozygous deletions of the GSTM1 and GSTT1 genes in women with sporadic breast cancer and in women without cancer and to compare breast cancer mammographic features between patients with and without these deletions.]. 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:18392488;
    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:NP43174.RAjByl_7OUCNkM0PL8cUuuLJ0beXCMiMFGRWDKCUs3Z9M130_publicationInfo {
  this: dct:created "2014-10-02T12:32:19+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" .
}