@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP806948.RArRqhAWQQrZrex-xVI2e3r9AonVFD2RCifNxzdw5YHYI> .
@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:NP806948.RArRqhAWQQrZrex-xVI2e3r9AonVFD2RCifNxzdw5YHYI130_head {
  this: np:hasAssertion dgn-np:NP806948.RArRqhAWQQrZrex-xVI2e3r9AonVFD2RCifNxzdw5YHYI130_assertion;
    np:hasProvenance dgn-np:NP806948.RArRqhAWQQrZrex-xVI2e3r9AonVFD2RCifNxzdw5YHYI130_provenance;
    np:hasPublicationInfo dgn-np:NP806948.RArRqhAWQQrZrex-xVI2e3r9AonVFD2RCifNxzdw5YHYI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP806948.RArRqhAWQQrZrex-xVI2e3r9AonVFD2RCifNxzdw5YHYI130_assertion a np:Assertion .
  
  dgn-np:NP806948.RArRqhAWQQrZrex-xVI2e3r9AonVFD2RCifNxzdw5YHYI130_provenance a np:Provenance .
  
  dgn-np:NP806948.RArRqhAWQQrZrex-xVI2e3r9AonVFD2RCifNxzdw5YHYI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP806948.RArRqhAWQQrZrex-xVI2e3r9AonVFD2RCifNxzdw5YHYI130_assertion {
  miriam-gene:8797 a ncit:C16612 .
  
  lld:C0266273 a ncit:C7057 .
  
  dgn-gda:DGNa847b0fc2fea808a0f068c350522f6fe sio:SIO_000628 miriam-gene:8797, lld:C0266273;
    a sio:SIO_001121 .
}

dgn-np:NP806948.RArRqhAWQQrZrex-xVI2e3r9AonVFD2RCifNxzdw5YHYI130_provenance {
  dgn-np:NP806948.RArRqhAWQQrZrex-xVI2e3r9AonVFD2RCifNxzdw5YHYI130_assertion dcterms:description
      "[In a study of 45 white patients from the United States with the disease, the relative risks (the number of times that an individual is at risk for Addison's disease if they had a marker, compared to those without such marker) were found to be 6.0, 4.6, and 26.5 for the DR3 allele, the DR4 allele, and for DR3/DR4 heterozygotes, respectively.]. 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:3484749;
    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:NP806948.RArRqhAWQQrZrex-xVI2e3r9AonVFD2RCifNxzdw5YHYI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:15+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" .
}