@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP58339.RA7lBO47zUcr9AALqdPI3rBa1aMVg5nffRqLt99jMsjCI> .
@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 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:NP58339.RA7lBO47zUcr9AALqdPI3rBa1aMVg5nffRqLt99jMsjCI130_head {
  this: np:hasAssertion dgn-np:NP58339.RA7lBO47zUcr9AALqdPI3rBa1aMVg5nffRqLt99jMsjCI130_assertion;
    np:hasProvenance dgn-np:NP58339.RA7lBO47zUcr9AALqdPI3rBa1aMVg5nffRqLt99jMsjCI130_provenance;
    np:hasPublicationInfo dgn-np:NP58339.RA7lBO47zUcr9AALqdPI3rBa1aMVg5nffRqLt99jMsjCI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP58339.RA7lBO47zUcr9AALqdPI3rBa1aMVg5nffRqLt99jMsjCI130_assertion a np:Assertion .
  
  dgn-np:NP58339.RA7lBO47zUcr9AALqdPI3rBa1aMVg5nffRqLt99jMsjCI130_provenance a np:Provenance .
  
  dgn-np:NP58339.RA7lBO47zUcr9AALqdPI3rBa1aMVg5nffRqLt99jMsjCI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP58339.RA7lBO47zUcr9AALqdPI3rBa1aMVg5nffRqLt99jMsjCI130_assertion {
  miriam-gene:3106 a ncit:C16612 .
  
  lld:C0029172 a ncit:C7057 .
  
  dgn-gda:DGN53b900f1b236fca05b965c9e67f233e9 sio:SIO_000628 miriam-gene:3106, lld:C0029172;
    a sio:SIO_001122 .
}

dgn-np:NP58339.RA7lBO47zUcr9AALqdPI3rBa1aMVg5nffRqLt99jMsjCI130_provenance {
  dgn-np:NP58339.RA7lBO47zUcr9AALqdPI3rBa1aMVg5nffRqLt99jMsjCI130_assertion dct:description
      "[ We conclude that some Taiwanese areca quid (AQ) chewers with particular HLA phenotypes and haplotypes are prone to have OSF. In addition, some particular HLA haplotypes may play more important roles than the individual HLA phenotypes for the genetic susceptibility to OSF. However, the significantly increased HLA phenotype B76 and three of the common HLA haplotypes detected are present in only about 20% of incident cases of OSF.]. 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:15061705;
    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:NP58339.RA7lBO47zUcr9AALqdPI3rBa1aMVg5nffRqLt99jMsjCI130_publicationInfo {
  this: dct:created "2014-10-02T12:32:27+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}