@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP44791.RAbBgVhdKk1MmOn-16qYXgQNrias2xqbjHwZHm4S9zqQY> .
@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:NP44791.RAbBgVhdKk1MmOn-16qYXgQNrias2xqbjHwZHm4S9zqQY130_head {
  this: np:hasAssertion dgn-np:NP44791.RAbBgVhdKk1MmOn-16qYXgQNrias2xqbjHwZHm4S9zqQY130_assertion;
    np:hasProvenance dgn-np:NP44791.RAbBgVhdKk1MmOn-16qYXgQNrias2xqbjHwZHm4S9zqQY130_provenance;
    np:hasPublicationInfo dgn-np:NP44791.RAbBgVhdKk1MmOn-16qYXgQNrias2xqbjHwZHm4S9zqQY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP44791.RAbBgVhdKk1MmOn-16qYXgQNrias2xqbjHwZHm4S9zqQY130_assertion a np:Assertion .
  
  dgn-np:NP44791.RAbBgVhdKk1MmOn-16qYXgQNrias2xqbjHwZHm4S9zqQY130_provenance a np:Provenance .
  
  dgn-np:NP44791.RAbBgVhdKk1MmOn-16qYXgQNrias2xqbjHwZHm4S9zqQY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP44791.RAbBgVhdKk1MmOn-16qYXgQNrias2xqbjHwZHm4S9zqQY130_assertion {
  miriam-gene:2099 a ncit:C16612 .
  
  lld:C0003873 a ncit:C7057 .
  
  dgn-gda:DGN9e7ec7d4157c806a7c098cd321abaff9 sio:SIO_000628 miriam-gene:2099, lld:C0003873;
    a sio:SIO_001122 .
}

dgn-np:NP44791.RAbBgVhdKk1MmOn-16qYXgQNrias2xqbjHwZHm4S9zqQY130_provenance {
  dgn-np:NP44791.RAbBgVhdKk1MmOn-16qYXgQNrias2xqbjHwZHm4S9zqQY130_assertion dcterms:description
      "[ Some variants of the OR gene are related to the onset of RA in women in certain age periods, suggesting the role of the interaction between the OR gene and serum concentrations of oestrogen at the onset of the disease.]. 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:10343533;
    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:NP44791.RAbBgVhdKk1MmOn-16qYXgQNrias2xqbjHwZHm4S9zqQY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:20+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" .
}