@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP768482.RAip32SuUmiXW-B5bQylJOdgXQSjO9xXt7Y14dcnPCcTM> .
@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:NP768482.RAip32SuUmiXW-B5bQylJOdgXQSjO9xXt7Y14dcnPCcTM130_head {
  this: np:hasAssertion dgn-np:NP768482.RAip32SuUmiXW-B5bQylJOdgXQSjO9xXt7Y14dcnPCcTM130_assertion;
    np:hasProvenance dgn-np:NP768482.RAip32SuUmiXW-B5bQylJOdgXQSjO9xXt7Y14dcnPCcTM130_provenance;
    np:hasPublicationInfo dgn-np:NP768482.RAip32SuUmiXW-B5bQylJOdgXQSjO9xXt7Y14dcnPCcTM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP768482.RAip32SuUmiXW-B5bQylJOdgXQSjO9xXt7Y14dcnPCcTM130_assertion a np:Assertion .
  
  dgn-np:NP768482.RAip32SuUmiXW-B5bQylJOdgXQSjO9xXt7Y14dcnPCcTM130_provenance a np:Provenance .
  
  dgn-np:NP768482.RAip32SuUmiXW-B5bQylJOdgXQSjO9xXt7Y14dcnPCcTM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP768482.RAip32SuUmiXW-B5bQylJOdgXQSjO9xXt7Y14dcnPCcTM130_assertion {
  miriam-gene:3123 a ncit:C16612 .
  
  lld:C0152171 a ncit:C7057 .
  
  dgn-gda:DGNb7bad28ded2c8c821be3b67e00b2e7a3 sio:SIO_000628 miriam-gene:3123, lld:C0152171;
    a sio:SIO_001121 .
}

dgn-np:NP768482.RAip32SuUmiXW-B5bQylJOdgXQSjO9xXt7Y14dcnPCcTM130_provenance {
  dgn-np:NP768482.RAip32SuUmiXW-B5bQylJOdgXQSjO9xXt7Y14dcnPCcTM130_assertion dcterms:description
      "[The aim of this study was to compare the frequency of the HLA-DRB1 and HLA-DQB1 alleles in Korean patients with idiopathic pulmonary arterial hypertension (IPAH) and in normal controls and to determine any association that may exist between clinical characteristics of IPAH and specific HLA alleles.]. 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:17406941;
    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:NP768482.RAip32SuUmiXW-B5bQylJOdgXQSjO9xXt7Y14dcnPCcTM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:45+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" .
}