@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP663858.RAS9MzfcmD1vgTDfLbKp3-I_7_OMKyuq5YcYKQZcwPuLc> .
@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:NP663858.RAS9MzfcmD1vgTDfLbKp3-I_7_OMKyuq5YcYKQZcwPuLc130_head {
  this: np:hasAssertion dgn-np:NP663858.RAS9MzfcmD1vgTDfLbKp3-I_7_OMKyuq5YcYKQZcwPuLc130_assertion;
    np:hasProvenance dgn-np:NP663858.RAS9MzfcmD1vgTDfLbKp3-I_7_OMKyuq5YcYKQZcwPuLc130_provenance;
    np:hasPublicationInfo dgn-np:NP663858.RAS9MzfcmD1vgTDfLbKp3-I_7_OMKyuq5YcYKQZcwPuLc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP663858.RAS9MzfcmD1vgTDfLbKp3-I_7_OMKyuq5YcYKQZcwPuLc130_assertion a np:Assertion .
  
  dgn-np:NP663858.RAS9MzfcmD1vgTDfLbKp3-I_7_OMKyuq5YcYKQZcwPuLc130_provenance a np:Provenance .
  
  dgn-np:NP663858.RAS9MzfcmD1vgTDfLbKp3-I_7_OMKyuq5YcYKQZcwPuLc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP663858.RAS9MzfcmD1vgTDfLbKp3-I_7_OMKyuq5YcYKQZcwPuLc130_assertion {
  miriam-gene:3126 a ncit:C16612 .
  
  lld:C0339143 a ncit:C7057 .
  
  dgn-gda:DGNc8976856651509091ad8b90ecf9df45c sio:SIO_000628 miriam-gene:3126, lld:C0339143;
    a sio:SIO_001121 .
}

dgn-np:NP663858.RAS9MzfcmD1vgTDfLbKp3-I_7_OMKyuq5YcYKQZcwPuLc130_provenance {
  dgn-np:NP663858.RAS9MzfcmD1vgTDfLbKp3-I_7_OMKyuq5YcYKQZcwPuLc130_assertion dcterms:description
      "[In an attempt to study the potential role of two non-HLA susceptibility alleles in GD and Graves' ophthalmopathy, we examined 286 North American Caucasian individuals (145 normal controls and 141 individuals with GD) for the presence of the A2 allele of the interleukin-1 (IL-1) receptor antagonist gene.]. 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:8954062;
    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:NP663858.RAS9MzfcmD1vgTDfLbKp3-I_7_OMKyuq5YcYKQZcwPuLc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:41+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" .
}