@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP318487.RADKOQ92r-dHD5GGAm1KSxBp7c8YTOyEy--rb2E8MjLUk> .
@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:NP318487.RADKOQ92r-dHD5GGAm1KSxBp7c8YTOyEy--rb2E8MjLUk130_head {
  this: np:hasAssertion dgn-np:NP318487.RADKOQ92r-dHD5GGAm1KSxBp7c8YTOyEy--rb2E8MjLUk130_assertion;
    np:hasProvenance dgn-np:NP318487.RADKOQ92r-dHD5GGAm1KSxBp7c8YTOyEy--rb2E8MjLUk130_provenance;
    np:hasPublicationInfo dgn-np:NP318487.RADKOQ92r-dHD5GGAm1KSxBp7c8YTOyEy--rb2E8MjLUk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP318487.RADKOQ92r-dHD5GGAm1KSxBp7c8YTOyEy--rb2E8MjLUk130_assertion a np:Assertion .
  
  dgn-np:NP318487.RADKOQ92r-dHD5GGAm1KSxBp7c8YTOyEy--rb2E8MjLUk130_provenance a np:Provenance .
  
  dgn-np:NP318487.RADKOQ92r-dHD5GGAm1KSxBp7c8YTOyEy--rb2E8MjLUk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP318487.RADKOQ92r-dHD5GGAm1KSxBp7c8YTOyEy--rb2E8MjLUk130_assertion {
  miriam-gene:57026 a ncit:C16612 .
  
  lld:C0280100 a ncit:C7057 .
  
  dgn-gda:DGN778ca40e15951ffe37c310c558c3a5e4 sio:SIO_000628 miriam-gene:57026, lld:C0280100;
    a sio:SIO_001121 .
}

dgn-np:NP318487.RADKOQ92r-dHD5GGAm1KSxBp7c8YTOyEy--rb2E8MjLUk130_provenance {
  dgn-np:NP318487.RADKOQ92r-dHD5GGAm1KSxBp7c8YTOyEy--rb2E8MjLUk130_assertion dcterms:description
      "[To gain more insight into the role of chromosomal instability (CIN), the cytogenetic hallmark of most solid tumors, we performed fluorescence in situ hybridization (FISH) on interphase nuclei of cytological specimens enabling the correct detection of chromosome copies in intact tumor cells of 18 well (G1), moderately (G2), or poorly (G3) differentiated hepatocellular carcinomas (HCCs).]. 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:14745031;
    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:NP318487.RADKOQ92r-dHD5GGAm1KSxBp7c8YTOyEy--rb2E8MjLUk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:04+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" .
}