@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP58531.RAb7gQznpS9VhWsFMfRvX0RbUBaLc6zEDKuo4xRzsheDU> .
@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:NP58531.RAb7gQznpS9VhWsFMfRvX0RbUBaLc6zEDKuo4xRzsheDU130_head {
  this: np:hasAssertion dgn-np:NP58531.RAb7gQznpS9VhWsFMfRvX0RbUBaLc6zEDKuo4xRzsheDU130_assertion;
    np:hasProvenance dgn-np:NP58531.RAb7gQznpS9VhWsFMfRvX0RbUBaLc6zEDKuo4xRzsheDU130_provenance;
    np:hasPublicationInfo dgn-np:NP58531.RAb7gQznpS9VhWsFMfRvX0RbUBaLc6zEDKuo4xRzsheDU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP58531.RAb7gQznpS9VhWsFMfRvX0RbUBaLc6zEDKuo4xRzsheDU130_assertion a np:Assertion .
  
  dgn-np:NP58531.RAb7gQznpS9VhWsFMfRvX0RbUBaLc6zEDKuo4xRzsheDU130_provenance a np:Provenance .
  
  dgn-np:NP58531.RAb7gQznpS9VhWsFMfRvX0RbUBaLc6zEDKuo4xRzsheDU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP58531.RAb7gQznpS9VhWsFMfRvX0RbUBaLc6zEDKuo4xRzsheDU130_assertion {
  miriam-gene:7133 a ncit:C16612 .
  
  lld:C0003873 a ncit:C7057 .
  
  dgn-gda:DGN0da339342ac9d0f6cb808f97f19fd244 sio:SIO_000628 miriam-gene:7133, lld:C0003873;
    a sio:SIO_001122 .
}

dgn-np:NP58531.RAb7gQznpS9VhWsFMfRvX0RbUBaLc6zEDKuo4xRzsheDU130_provenance {
  dgn-np:NP58531.RAb7gQznpS9VhWsFMfRvX0RbUBaLc6zEDKuo4xRzsheDU130_assertion dcterms: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:NP58531.RAb7gQznpS9VhWsFMfRvX0RbUBaLc6zEDKuo4xRzsheDU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:27+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" .
}