@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP398572.RAv2KIiH7-rUPqR7JS8VKmBynoZsi50_TSyEMn85E3MJI> .
@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:NP398572.RAv2KIiH7-rUPqR7JS8VKmBynoZsi50_TSyEMn85E3MJI130_head {
  this: np:hasAssertion dgn-np:NP398572.RAv2KIiH7-rUPqR7JS8VKmBynoZsi50_TSyEMn85E3MJI130_assertion ;
    np:hasProvenance dgn-np:NP398572.RAv2KIiH7-rUPqR7JS8VKmBynoZsi50_TSyEMn85E3MJI130_provenance ;
    np:hasPublicationInfo dgn-np:NP398572.RAv2KIiH7-rUPqR7JS8VKmBynoZsi50_TSyEMn85E3MJI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP398572.RAv2KIiH7-rUPqR7JS8VKmBynoZsi50_TSyEMn85E3MJI130_assertion a np:Assertion .
  dgn-np:NP398572.RAv2KIiH7-rUPqR7JS8VKmBynoZsi50_TSyEMn85E3MJI130_provenance a np:Provenance .
  dgn-np:NP398572.RAv2KIiH7-rUPqR7JS8VKmBynoZsi50_TSyEMn85E3MJI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP398572.RAv2KIiH7-rUPqR7JS8VKmBynoZsi50_TSyEMn85E3MJI130_assertion {
  miriam-gene:4810 a ncit:C16612 .
  lld:C0003873 a ncit:C7057 .
  dgn-gda:DGN9f285ab6046e44ef7a80057b2cc17b8f sio:SIO_000628 miriam-gene:4810 , lld:C0003873 ;
    a sio:SIO_001121 .
}
dgn-np:NP398572.RAv2KIiH7-rUPqR7JS8VKmBynoZsi50_TSyEMn85E3MJI130_provenance {
  dgn-np:NP398572.RAv2KIiH7-rUPqR7JS8VKmBynoZsi50_TSyEMn85E3MJI130_assertion dcterms:description "[We genotyped AR, ESR2, CYP19, PGR SNPs and the AR CAG repeat in RA case-control studies nested within the Nurses' Health Study (NHS), NHS II (449 RA cases, 449 controls) and the Women's Health Study (72 cases, and 202 controls).]. 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:19555469 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP398572.RAv2KIiH7-rUPqR7JS8VKmBynoZsi50_TSyEMn85E3MJI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:57+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> ;
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}