@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP164212.RA7on9CPL_NlGxkvrgcCQvrHgXhLkj0Ki6cSbB_A_CjBY> .
@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:NP164212.RA7on9CPL_NlGxkvrgcCQvrHgXhLkj0Ki6cSbB_A_CjBY130_head {
  this: np:hasAssertion dgn-np:NP164212.RA7on9CPL_NlGxkvrgcCQvrHgXhLkj0Ki6cSbB_A_CjBY130_assertion;
    np:hasProvenance dgn-np:NP164212.RA7on9CPL_NlGxkvrgcCQvrHgXhLkj0Ki6cSbB_A_CjBY130_provenance;
    np:hasPublicationInfo dgn-np:NP164212.RA7on9CPL_NlGxkvrgcCQvrHgXhLkj0Ki6cSbB_A_CjBY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP164212.RA7on9CPL_NlGxkvrgcCQvrHgXhLkj0Ki6cSbB_A_CjBY130_assertion a np:Assertion .
  
  dgn-np:NP164212.RA7on9CPL_NlGxkvrgcCQvrHgXhLkj0Ki6cSbB_A_CjBY130_provenance a np:Provenance .
  
  dgn-np:NP164212.RA7on9CPL_NlGxkvrgcCQvrHgXhLkj0Ki6cSbB_A_CjBY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP164212.RA7on9CPL_NlGxkvrgcCQvrHgXhLkj0Ki6cSbB_A_CjBY130_assertion {
  miriam-gene:3342 a ncit:C16612 .
  
  lld:C2239176 a ncit:C7057 .
  
  dgn-gda:DGNed33b1cb2f17a95f170ab36dac9006a7 sio:SIO_000628 miriam-gene:3342, lld:C2239176;
    a sio:SIO_001121 .
}

dgn-np:NP164212.RA7on9CPL_NlGxkvrgcCQvrHgXhLkj0Ki6cSbB_A_CjBY130_provenance {
  dgn-np:NP164212.RA7on9CPL_NlGxkvrgcCQvrHgXhLkj0Ki6cSbB_A_CjBY130_assertion dcterms:description
      "[In conclusion, this study shows that array-based CGH provides high resolution mapping of chromosomal aberrations in HCC, and demonstrates the feasibility of correlating array CGH data with gene expression data to identify novel oncogenes and tumor suppressor genes.]. 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:16000397;
    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:NP164212.RA7on9CPL_NlGxkvrgcCQvrHgXhLkj0Ki6cSbB_A_CjBY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:29+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" .
}