@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP912274.RAPiKZ2p5AWmf5n8O2ZQB4fHLV0-pVSwW1I6Kn4I02ri8> .
@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:NP912274.RAPiKZ2p5AWmf5n8O2ZQB4fHLV0-pVSwW1I6Kn4I02ri8130_head {
  this: np:hasAssertion dgn-np:NP912274.RAPiKZ2p5AWmf5n8O2ZQB4fHLV0-pVSwW1I6Kn4I02ri8130_assertion;
    np:hasProvenance dgn-np:NP912274.RAPiKZ2p5AWmf5n8O2ZQB4fHLV0-pVSwW1I6Kn4I02ri8130_provenance;
    np:hasPublicationInfo dgn-np:NP912274.RAPiKZ2p5AWmf5n8O2ZQB4fHLV0-pVSwW1I6Kn4I02ri8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP912274.RAPiKZ2p5AWmf5n8O2ZQB4fHLV0-pVSwW1I6Kn4I02ri8130_assertion a np:Assertion .
  
  dgn-np:NP912274.RAPiKZ2p5AWmf5n8O2ZQB4fHLV0-pVSwW1I6Kn4I02ri8130_provenance a np:Provenance .
  
  dgn-np:NP912274.RAPiKZ2p5AWmf5n8O2ZQB4fHLV0-pVSwW1I6Kn4I02ri8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP912274.RAPiKZ2p5AWmf5n8O2ZQB4fHLV0-pVSwW1I6Kn4I02ri8130_assertion {
  miriam-gene:728655 a ncit:C16612 .
  
  lld:C0151317 a ncit:C7057 .
  
  dgn-gda:DGN8eb5ae2e173d25066d9b1fd16879ab5c sio:SIO_000628 miriam-gene:728655, lld:C0151317;
    a sio:SIO_001121 .
}

dgn-np:NP912274.RAPiKZ2p5AWmf5n8O2ZQB4fHLV0-pVSwW1I6Kn4I02ri8130_provenance {
  dgn-np:NP912274.RAPiKZ2p5AWmf5n8O2ZQB4fHLV0-pVSwW1I6Kn4I02ri8130_assertion dcterms:description
      "[We conducted a case-control study and genotyped two SNPs, rs7763881 in HULC and rs619586 in MALAT1, in 1300 HBV positive HCC patients, 1344 HBV persistent carriers and 1344 subjects with HBV natural clearance to test the associations between the two SNPs and susceptibility to HCC and HBV chronic infection.]. 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:22493738;
    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:NP912274.RAPiKZ2p5AWmf5n8O2ZQB4fHLV0-pVSwW1I6Kn4I02ri8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:20+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" .
}