@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP46533.RAI95gx7_tEU8rH_ysr3Vy4DAGyDVXPjtkq_4UvH3jpz4> .
@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:NP46533.RAI95gx7_tEU8rH_ysr3Vy4DAGyDVXPjtkq_4UvH3jpz4130_head {
  this: np:hasAssertion dgn-np:NP46533.RAI95gx7_tEU8rH_ysr3Vy4DAGyDVXPjtkq_4UvH3jpz4130_assertion;
    np:hasProvenance dgn-np:NP46533.RAI95gx7_tEU8rH_ysr3Vy4DAGyDVXPjtkq_4UvH3jpz4130_provenance;
    np:hasPublicationInfo dgn-np:NP46533.RAI95gx7_tEU8rH_ysr3Vy4DAGyDVXPjtkq_4UvH3jpz4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP46533.RAI95gx7_tEU8rH_ysr3Vy4DAGyDVXPjtkq_4UvH3jpz4130_assertion a np:Assertion .
  
  dgn-np:NP46533.RAI95gx7_tEU8rH_ysr3Vy4DAGyDVXPjtkq_4UvH3jpz4130_provenance a np:Provenance .
  
  dgn-np:NP46533.RAI95gx7_tEU8rH_ysr3Vy4DAGyDVXPjtkq_4UvH3jpz4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP46533.RAI95gx7_tEU8rH_ysr3Vy4DAGyDVXPjtkq_4UvH3jpz4130_assertion {
  miriam-gene:1565 a ncit:C16612 .
  
  lld:C0001403 a ncit:C7057 .
  
  dgn-gda:DGN2d818d932f0b2af4b5f7a11200c2891a sio:SIO_000628 miriam-gene:1565, lld:C0001403;
    a sio:SIO_001122 .
}

dgn-np:NP46533.RAI95gx7_tEU8rH_ysr3Vy4DAGyDVXPjtkq_4UvH3jpz4130_provenance {
  dgn-np:NP46533.RAI95gx7_tEU8rH_ysr3Vy4DAGyDVXPjtkq_4UvH3jpz4130_assertion dcterms:description
      "[ These results indicate that differences exist in the frequency of the 106 base pair allele in different population groups and in only the English population was the 106 base pair allele associated with Addison's disease.]. 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:10197076;
    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:NP46533.RAI95gx7_tEU8rH_ysr3Vy4DAGyDVXPjtkq_4UvH3jpz4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:21+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" .
}