@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP46158.RAnuQpy7vBTE4eNI22yGccgwZGsH0DouTbvQHwO3FUdBk> .
@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:NP46158.RAnuQpy7vBTE4eNI22yGccgwZGsH0DouTbvQHwO3FUdBk130_head {
  this: np:hasAssertion dgn-np:NP46158.RAnuQpy7vBTE4eNI22yGccgwZGsH0DouTbvQHwO3FUdBk130_assertion;
    np:hasProvenance dgn-np:NP46158.RAnuQpy7vBTE4eNI22yGccgwZGsH0DouTbvQHwO3FUdBk130_provenance;
    np:hasPublicationInfo dgn-np:NP46158.RAnuQpy7vBTE4eNI22yGccgwZGsH0DouTbvQHwO3FUdBk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP46158.RAnuQpy7vBTE4eNI22yGccgwZGsH0DouTbvQHwO3FUdBk130_assertion a np:Assertion .
  
  dgn-np:NP46158.RAnuQpy7vBTE4eNI22yGccgwZGsH0DouTbvQHwO3FUdBk130_provenance a np:Provenance .
  
  dgn-np:NP46158.RAnuQpy7vBTE4eNI22yGccgwZGsH0DouTbvQHwO3FUdBk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP46158.RAnuQpy7vBTE4eNI22yGccgwZGsH0DouTbvQHwO3FUdBk130_assertion {
  miriam-gene:1588 a ncit:C16612 .
  
  lld:C0006142 a ncit:C7057 .
  
  dgn-gda:DGN9d02f37e7ec7fd273fa560822d1359c2 sio:SIO_000628 miriam-gene:1588, lld:C0006142;
    a sio:SIO_001122 .
}

dgn-np:NP46158.RAnuQpy7vBTE4eNI22yGccgwZGsH0DouTbvQHwO3FUdBk130_provenance {
  dgn-np:NP46158.RAnuQpy7vBTE4eNI22yGccgwZGsH0DouTbvQHwO3FUdBk130_assertion dct:description
      "[Pairwise analysis showed that combinations of the ERalpha G allele with the homozygous Trp genotype of CYP19A1 codon 39 (rs2236722), the methionine (Met) allele of COMT codon 158 (rs4680) or Pro allele of p53 codon 72 (rs1042522) were more frequent in ER-positive than ER-negative breast cancer, especially in patients less than 50-year old.]. 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:18820009;
    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:NP46158.RAnuQpy7vBTE4eNI22yGccgwZGsH0DouTbvQHwO3FUdBk130_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" .
}