@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP188019.RA5ESnf_E6Rqa_1Xjv2J173nHW0m8bMbFQDvvn5l0BMsg> .
@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:NP188019.RA5ESnf_E6Rqa_1Xjv2J173nHW0m8bMbFQDvvn5l0BMsg130_head {
  this: np:hasAssertion dgn-np:NP188019.RA5ESnf_E6Rqa_1Xjv2J173nHW0m8bMbFQDvvn5l0BMsg130_assertion;
    np:hasProvenance dgn-np:NP188019.RA5ESnf_E6Rqa_1Xjv2J173nHW0m8bMbFQDvvn5l0BMsg130_provenance;
    np:hasPublicationInfo dgn-np:NP188019.RA5ESnf_E6Rqa_1Xjv2J173nHW0m8bMbFQDvvn5l0BMsg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP188019.RA5ESnf_E6Rqa_1Xjv2J173nHW0m8bMbFQDvvn5l0BMsg130_assertion a np:Assertion .
  
  dgn-np:NP188019.RA5ESnf_E6Rqa_1Xjv2J173nHW0m8bMbFQDvvn5l0BMsg130_provenance a np:Provenance .
  
  dgn-np:NP188019.RA5ESnf_E6Rqa_1Xjv2J173nHW0m8bMbFQDvvn5l0BMsg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP188019.RA5ESnf_E6Rqa_1Xjv2J173nHW0m8bMbFQDvvn5l0BMsg130_assertion {
  miriam-gene:1861 a ncit:C16612 .
  
  lld:C0266273 a ncit:C7057 .
  
  dgn-gda:DGN1b5abdd9717aa2bb89074b1dbc7ba5d7 sio:SIO_000628 miriam-gene:1861, lld:C0266273;
    a sio:SIO_001121 .
}

dgn-np:NP188019.RA5ESnf_E6Rqa_1Xjv2J173nHW0m8bMbFQDvvn5l0BMsg130_provenance {
  dgn-np:NP188019.RA5ESnf_E6Rqa_1Xjv2J173nHW0m8bMbFQDvvn5l0BMsg130_assertion dcterms:description
      "[In the current study, we ascertained the haplotypes of 57 Caucasian patients with Addison's disease composed of these genetic markers and compared them either with 72 general population controls or with 105 child controls carrying Addison's disease high-risk DR3-DQ2/DR4-DQ8 genotypes.]. 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:12392510;
    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:NP188019.RA5ESnf_E6Rqa_1Xjv2J173nHW0m8bMbFQDvvn5l0BMsg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:43+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" .
}