@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP46250.RApiG8RpFa2mP4RNBXsnJ6P1N82JoDDi4OzxN4F_w1uwM> .
@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:NP46250.RApiG8RpFa2mP4RNBXsnJ6P1N82JoDDi4OzxN4F_w1uwM130_head {
  this: np:hasAssertion dgn-np:NP46250.RApiG8RpFa2mP4RNBXsnJ6P1N82JoDDi4OzxN4F_w1uwM130_assertion;
    np:hasProvenance dgn-np:NP46250.RApiG8RpFa2mP4RNBXsnJ6P1N82JoDDi4OzxN4F_w1uwM130_provenance;
    np:hasPublicationInfo dgn-np:NP46250.RApiG8RpFa2mP4RNBXsnJ6P1N82JoDDi4OzxN4F_w1uwM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP46250.RApiG8RpFa2mP4RNBXsnJ6P1N82JoDDi4OzxN4F_w1uwM130_assertion a np:Assertion .
  
  dgn-np:NP46250.RApiG8RpFa2mP4RNBXsnJ6P1N82JoDDi4OzxN4F_w1uwM130_provenance a np:Provenance .
  
  dgn-np:NP46250.RApiG8RpFa2mP4RNBXsnJ6P1N82JoDDi4OzxN4F_w1uwM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP46250.RApiG8RpFa2mP4RNBXsnJ6P1N82JoDDi4OzxN4F_w1uwM130_assertion {
  miriam-gene:1586 a ncit:C16612 .
  
  lld:C0003873 a ncit:C7057 .
  
  dgn-gda:DGN32e22a4cb177c44080393b49d11771cf sio:SIO_000628 miriam-gene:1586, lld:C0003873;
    a sio:SIO_001122 .
}

dgn-np:NP46250.RApiG8RpFa2mP4RNBXsnJ6P1N82JoDDi4OzxN4F_w1uwM130_provenance {
  dgn-np:NP46250.RApiG8RpFa2mP4RNBXsnJ6P1N82JoDDi4OzxN4F_w1uwM130_assertion dct:description
      "[This study suggests that the A2 allele may significantly decrease the overall risk of developing RA. In women, the protective effect of A2 mainly affects the older age group. In men, the clinical severity of RA may decrease in patients with the A2/A2 genotype.]. 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:15235815;
    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:NP46250.RApiG8RpFa2mP4RNBXsnJ6P1N82JoDDi4OzxN4F_w1uwM130_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" .
}