@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP58556.RAmRD8s5qKba5iJCO6kBZVECh_5uLvTkc0BKomgP63gbU> .
@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:NP58556.RAmRD8s5qKba5iJCO6kBZVECh_5uLvTkc0BKomgP63gbU130_head {
  this: np:hasAssertion dgn-np:NP58556.RAmRD8s5qKba5iJCO6kBZVECh_5uLvTkc0BKomgP63gbU130_assertion;
    np:hasProvenance dgn-np:NP58556.RAmRD8s5qKba5iJCO6kBZVECh_5uLvTkc0BKomgP63gbU130_provenance;
    np:hasPublicationInfo dgn-np:NP58556.RAmRD8s5qKba5iJCO6kBZVECh_5uLvTkc0BKomgP63gbU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP58556.RAmRD8s5qKba5iJCO6kBZVECh_5uLvTkc0BKomgP63gbU130_assertion a np:Assertion .
  
  dgn-np:NP58556.RAmRD8s5qKba5iJCO6kBZVECh_5uLvTkc0BKomgP63gbU130_provenance a np:Provenance .
  
  dgn-np:NP58556.RAmRD8s5qKba5iJCO6kBZVECh_5uLvTkc0BKomgP63gbU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP58556.RAmRD8s5qKba5iJCO6kBZVECh_5uLvTkc0BKomgP63gbU130_assertion {
  miriam-gene:7133 a ncit:C16612 .
  
  lld:C0003864 a ncit:C7057 .
  
  dgn-gda:DGNa2a3d113c459c08288b6ae4ff8b08c42 sio:SIO_000628 miriam-gene:7133, lld:C0003864;
    a sio:SIO_001122 .
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dgn-np:NP58556.RAmRD8s5qKba5iJCO6kBZVECh_5uLvTkc0BKomgP63gbU130_provenance {
  dgn-np:NP58556.RAmRD8s5qKba5iJCO6kBZVECh_5uLvTkc0BKomgP63gbU130_assertion dcterms:description
      "[ Although we observed no associations between known TNFR SNPs or haplotypes and RA, significant racial differences were observed at both loci. Comparison of these data with other published frequencies of TNFRSF1A and TNFRSF1B genotypes according to race suggests that the distribution in African American, Caucasian, and Asian populations differs significantly. These striking racial/ethnic differences in TNFR SNP frequencies may influence the likelihood of familial RA, severe disease, or response to TNF inhibitors and may have important evolutionary implications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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    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:NP58556.RAmRD8s5qKba5iJCO6kBZVECh_5uLvTkc0BKomgP63gbU130_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>;
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    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
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