@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP326583.RAHv29JAzv-JD8RqHO_fceKIchl5sXdpCuWbtQ2RaeRNA> .
@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:NP326583.RAHv29JAzv-JD8RqHO_fceKIchl5sXdpCuWbtQ2RaeRNA130_head {
  this: np:hasAssertion dgn-np:NP326583.RAHv29JAzv-JD8RqHO_fceKIchl5sXdpCuWbtQ2RaeRNA130_assertion;
    np:hasProvenance dgn-np:NP326583.RAHv29JAzv-JD8RqHO_fceKIchl5sXdpCuWbtQ2RaeRNA130_provenance;
    np:hasPublicationInfo dgn-np:NP326583.RAHv29JAzv-JD8RqHO_fceKIchl5sXdpCuWbtQ2RaeRNA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP326583.RAHv29JAzv-JD8RqHO_fceKIchl5sXdpCuWbtQ2RaeRNA130_assertion a np:Assertion .
  
  dgn-np:NP326583.RAHv29JAzv-JD8RqHO_fceKIchl5sXdpCuWbtQ2RaeRNA130_provenance a np:Provenance .
  
  dgn-np:NP326583.RAHv29JAzv-JD8RqHO_fceKIchl5sXdpCuWbtQ2RaeRNA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP326583.RAHv29JAzv-JD8RqHO_fceKIchl5sXdpCuWbtQ2RaeRNA130_assertion {
  miriam-gene:11102 a ncit:C16612 .
  
  lld:C2239176 a ncit:C7057 .
  
  dgn-gda:DGN10b12443e886a85993062ccf4d961100 sio:SIO_000628 miriam-gene:11102, lld:C2239176;
    a sio:SIO_001121 .
}

dgn-np:NP326583.RAHv29JAzv-JD8RqHO_fceKIchl5sXdpCuWbtQ2RaeRNA130_provenance {
  dgn-np:NP326583.RAHv29JAzv-JD8RqHO_fceKIchl5sXdpCuWbtQ2RaeRNA130_assertion dcterms:description
      "[These results suggest that p14(ARF), p16(INK4a) and p53 are differentially disrupted through distinct molecular mechanisms at different stages in HCC and that p14(ARF) and p53 appear to function in the same tumor suppression pathway in HCC]. 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:12168936;
    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:NP326583.RAHv29JAzv-JD8RqHO_fceKIchl5sXdpCuWbtQ2RaeRNA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:11+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" .
}