@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP57807.RAB6icuJQ_zTV5v42PKfaFRvLLTy-MPYtmkGMQbubFSsE> .
@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:NP57807.RAB6icuJQ_zTV5v42PKfaFRvLLTy-MPYtmkGMQbubFSsE130_head {
  this: np:hasAssertion dgn-np:NP57807.RAB6icuJQ_zTV5v42PKfaFRvLLTy-MPYtmkGMQbubFSsE130_assertion;
    np:hasProvenance dgn-np:NP57807.RAB6icuJQ_zTV5v42PKfaFRvLLTy-MPYtmkGMQbubFSsE130_provenance;
    np:hasPublicationInfo dgn-np:NP57807.RAB6icuJQ_zTV5v42PKfaFRvLLTy-MPYtmkGMQbubFSsE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP57807.RAB6icuJQ_zTV5v42PKfaFRvLLTy-MPYtmkGMQbubFSsE130_assertion a np:Assertion .
  
  dgn-np:NP57807.RAB6icuJQ_zTV5v42PKfaFRvLLTy-MPYtmkGMQbubFSsE130_provenance a np:Provenance .
  
  dgn-np:NP57807.RAB6icuJQ_zTV5v42PKfaFRvLLTy-MPYtmkGMQbubFSsE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP57807.RAB6icuJQ_zTV5v42PKfaFRvLLTy-MPYtmkGMQbubFSsE130_assertion {
  miriam-gene:3119 a ncit:C16612 .
  
  lld:C0029172 a ncit:C7057 .
  
  dgn-gda:DGN524926015a9fef000493f497bed87be7 sio:SIO_000628 miriam-gene:3119, lld:C0029172;
    a sio:SIO_001122 .
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dgn-np:NP57807.RAB6icuJQ_zTV5v42PKfaFRvLLTy-MPYtmkGMQbubFSsE130_provenance {
  dgn-np:NP57807.RAB6icuJQ_zTV5v42PKfaFRvLLTy-MPYtmkGMQbubFSsE130_assertion dcterms: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:NP57807.RAB6icuJQ_zTV5v42PKfaFRvLLTy-MPYtmkGMQbubFSsE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:27+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" .
}