@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP523675.RAhJYBGOyob7Pe3g77No5EqTk6jDHZ0PuyrbvCmIqpXbg> .
@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:NP523675.RAhJYBGOyob7Pe3g77No5EqTk6jDHZ0PuyrbvCmIqpXbg130_head {
  this: np:hasAssertion dgn-np:NP523675.RAhJYBGOyob7Pe3g77No5EqTk6jDHZ0PuyrbvCmIqpXbg130_assertion;
    np:hasProvenance dgn-np:NP523675.RAhJYBGOyob7Pe3g77No5EqTk6jDHZ0PuyrbvCmIqpXbg130_provenance;
    np:hasPublicationInfo dgn-np:NP523675.RAhJYBGOyob7Pe3g77No5EqTk6jDHZ0PuyrbvCmIqpXbg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP523675.RAhJYBGOyob7Pe3g77No5EqTk6jDHZ0PuyrbvCmIqpXbg130_assertion a np:Assertion .
  
  dgn-np:NP523675.RAhJYBGOyob7Pe3g77No5EqTk6jDHZ0PuyrbvCmIqpXbg130_provenance a np:Provenance .
  
  dgn-np:NP523675.RAhJYBGOyob7Pe3g77No5EqTk6jDHZ0PuyrbvCmIqpXbg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP523675.RAhJYBGOyob7Pe3g77No5EqTk6jDHZ0PuyrbvCmIqpXbg130_assertion {
  miriam-gene:8170 a ncit:C16612 .
  
  lld:C0019163 a ncit:C7057 .
  
  dgn-gda:DGN5f97ae4beff7212b09399a8cf7e50942 sio:SIO_000628 miriam-gene:8170, lld:C0019163;
    a sio:SIO_001121 .
}

dgn-np:NP523675.RAhJYBGOyob7Pe3g77No5EqTk6jDHZ0PuyrbvCmIqpXbg130_provenance {
  dgn-np:NP523675.RAhJYBGOyob7Pe3g77No5EqTk6jDHZ0PuyrbvCmIqpXbg130_assertion dcterms:description
      "[The associations between seven common GRP78 polymorphisms in the promoter (rs391957, rs17840762, rs17840761, rs11355458) and in the 3' untranslated region (UTR) (rs16927997, rs1140763, rs12009) and possible risk of chronic HBV infection were assessed in a case-control study.]. 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:20525207;
    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:NP523675.RAhJYBGOyob7Pe3g77No5EqTk6jDHZ0PuyrbvCmIqpXbg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:14+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" .
}