@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP58505.RA_-bsxj5fqLKiM9jTnbGf49cNn8Mk4QUNiPX2lNnDy-M> .
@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:NP58505.RA_-bsxj5fqLKiM9jTnbGf49cNn8Mk4QUNiPX2lNnDy-M130_head {
  this: np:hasAssertion dgn-np:NP58505.RA_-bsxj5fqLKiM9jTnbGf49cNn8Mk4QUNiPX2lNnDy-M130_assertion;
    np:hasProvenance dgn-np:NP58505.RA_-bsxj5fqLKiM9jTnbGf49cNn8Mk4QUNiPX2lNnDy-M130_provenance;
    np:hasPublicationInfo dgn-np:NP58505.RA_-bsxj5fqLKiM9jTnbGf49cNn8Mk4QUNiPX2lNnDy-M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP58505.RA_-bsxj5fqLKiM9jTnbGf49cNn8Mk4QUNiPX2lNnDy-M130_assertion a np:Assertion .
  
  dgn-np:NP58505.RA_-bsxj5fqLKiM9jTnbGf49cNn8Mk4QUNiPX2lNnDy-M130_provenance a np:Provenance .
  
  dgn-np:NP58505.RA_-bsxj5fqLKiM9jTnbGf49cNn8Mk4QUNiPX2lNnDy-M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP58505.RA_-bsxj5fqLKiM9jTnbGf49cNn8Mk4QUNiPX2lNnDy-M130_assertion {
  miriam-gene:7132 a ncit:C16612 .
  
  lld:C0003873 a ncit:C7057 .
  
  dgn-gda:DGN1f7dea5c02484eb15bdae6aed420ebd1 sio:SIO_000628 miriam-gene:7132, lld:C0003873;
    a sio:SIO_001122 .
}

dgn-np:NP58505.RA_-bsxj5fqLKiM9jTnbGf49cNn8Mk4QUNiPX2lNnDy-M130_provenance {
  dgn-np:NP58505.RA_-bsxj5fqLKiM9jTnbGf49cNn8Mk4QUNiPX2lNnDy-M130_assertion dct:description
      "[ Genetic variation in the HLA-DRB1 and the LTA-TNF regions is significantly associated with response to treatment of early RA. These findings may have clinical application through the identification of patients who are most likely to benefit from treatment with methotrexate or etanercept.]. 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:15457442;
    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:NP58505.RA_-bsxj5fqLKiM9jTnbGf49cNn8Mk4QUNiPX2lNnDy-M130_publicationInfo {
  this: dct:created "2014-10-02T12:32:27+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" .
}