@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP50977.RAdEo2WPmnThtb7xl7wa54BlLdXNorfI_tnPyJoSmwgG4> .
@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:NP50977.RAdEo2WPmnThtb7xl7wa54BlLdXNorfI_tnPyJoSmwgG4130_head {
  this: np:hasAssertion dgn-np:NP50977.RAdEo2WPmnThtb7xl7wa54BlLdXNorfI_tnPyJoSmwgG4130_assertion;
    np:hasProvenance dgn-np:NP50977.RAdEo2WPmnThtb7xl7wa54BlLdXNorfI_tnPyJoSmwgG4130_provenance;
    np:hasPublicationInfo dgn-np:NP50977.RAdEo2WPmnThtb7xl7wa54BlLdXNorfI_tnPyJoSmwgG4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP50977.RAdEo2WPmnThtb7xl7wa54BlLdXNorfI_tnPyJoSmwgG4130_assertion a np:Assertion .
  
  dgn-np:NP50977.RAdEo2WPmnThtb7xl7wa54BlLdXNorfI_tnPyJoSmwgG4130_provenance a np:Provenance .
  
  dgn-np:NP50977.RAdEo2WPmnThtb7xl7wa54BlLdXNorfI_tnPyJoSmwgG4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP50977.RAdEo2WPmnThtb7xl7wa54BlLdXNorfI_tnPyJoSmwgG4130_assertion {
  miriam-gene:6817 a ncit:C16612 .
  
  lld:C0006142 a ncit:C7057 .
  
  dgn-gda:DGN8811e783565294fe16dfd6b6e7add6fd sio:SIO_000628 miriam-gene:6817, lld:C0006142;
    a sio:SIO_001122 .
}

dgn-np:NP50977.RAdEo2WPmnThtb7xl7wa54BlLdXNorfI_tnPyJoSmwgG4130_provenance {
  dgn-np:NP50977.RAdEo2WPmnThtb7xl7wa54BlLdXNorfI_tnPyJoSmwgG4130_assertion dcterms:description
      "[We concluded that the polymorphism of SULT1A1 Arg213His might be one of the high risk factors for breast cancer in Asian women and in postmenopausal women for all races. We should point out that the publication bias among postmenopausal women may partly account for the result, but the conclusion might not affected deeply by the publication bias.]. 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:20663177;
    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:NP50977.RAdEo2WPmnThtb7xl7wa54BlLdXNorfI_tnPyJoSmwgG4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:23+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" .
}