@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP339279.RAvHyRy7X_8-1h9RkTy6FQMZ_H5tnYiEqjIonREMc4cBw> .
@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:NP339279.RAvHyRy7X_8-1h9RkTy6FQMZ_H5tnYiEqjIonREMc4cBw130_head {
  this: np:hasAssertion dgn-np:NP339279.RAvHyRy7X_8-1h9RkTy6FQMZ_H5tnYiEqjIonREMc4cBw130_assertion ;
    np:hasProvenance dgn-np:NP339279.RAvHyRy7X_8-1h9RkTy6FQMZ_H5tnYiEqjIonREMc4cBw130_provenance ;
    np:hasPublicationInfo dgn-np:NP339279.RAvHyRy7X_8-1h9RkTy6FQMZ_H5tnYiEqjIonREMc4cBw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP339279.RAvHyRy7X_8-1h9RkTy6FQMZ_H5tnYiEqjIonREMc4cBw130_assertion a np:Assertion .
  dgn-np:NP339279.RAvHyRy7X_8-1h9RkTy6FQMZ_H5tnYiEqjIonREMc4cBw130_provenance a np:Provenance .
  dgn-np:NP339279.RAvHyRy7X_8-1h9RkTy6FQMZ_H5tnYiEqjIonREMc4cBw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP339279.RAvHyRy7X_8-1h9RkTy6FQMZ_H5tnYiEqjIonREMc4cBw130_assertion {
  miriam-gene:597 a ncit:C16612 .
  lld:C0003873 a ncit:C7057 .
  dgn-gda:DGNcc49358510dae858e844c3ab81ee480a sio:SIO_000628 miriam-gene:597 , lld:C0003873 ;
    a sio:SIO_001121 .
}
dgn-np:NP339279.RAvHyRy7X_8-1h9RkTy6FQMZ_H5tnYiEqjIonREMc4cBw130_provenance {
  dgn-np:NP339279.RAvHyRy7X_8-1h9RkTy6FQMZ_H5tnYiEqjIonREMc4cBw130_assertion dcterms:description "[In 1,515 EHR-derived RA cases and 1,480 controls matched for both genetic ancestry and disease-specific autoantibodies (anti-citrullinated protein antibodies [ACPA]), we demonstrate that the odds ratios and aggregate genetic risk score (GRS) of known RA risk alleles measured in individuals of European ancestry within our EHR cohort are nearly identical to those derived from a genome-wide association study (GWAS) of 5,539 autoantibody-positive RA cases and 20,169 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:21211616 ;
    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:NP339279.RAvHyRy7X_8-1h9RkTy6FQMZ_H5tnYiEqjIonREMc4cBw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:19+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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}