@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP181412.RAXv6aXggSt1DPdKl_nMPcHkwDO7W-Y6aCPVfmEIRCT00> .
@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:NP181412.RAXv6aXggSt1DPdKl_nMPcHkwDO7W-Y6aCPVfmEIRCT00130_head {
  this: np:hasAssertion dgn-np:NP181412.RAXv6aXggSt1DPdKl_nMPcHkwDO7W-Y6aCPVfmEIRCT00130_assertion;
    np:hasProvenance dgn-np:NP181412.RAXv6aXggSt1DPdKl_nMPcHkwDO7W-Y6aCPVfmEIRCT00130_provenance;
    np:hasPublicationInfo dgn-np:NP181412.RAXv6aXggSt1DPdKl_nMPcHkwDO7W-Y6aCPVfmEIRCT00130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP181412.RAXv6aXggSt1DPdKl_nMPcHkwDO7W-Y6aCPVfmEIRCT00130_assertion a np:Assertion .
  
  dgn-np:NP181412.RAXv6aXggSt1DPdKl_nMPcHkwDO7W-Y6aCPVfmEIRCT00130_provenance a np:Provenance .
  
  dgn-np:NP181412.RAXv6aXggSt1DPdKl_nMPcHkwDO7W-Y6aCPVfmEIRCT00130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP181412.RAXv6aXggSt1DPdKl_nMPcHkwDO7W-Y6aCPVfmEIRCT00130_assertion {
  miriam-gene:1021 a ncit:C16612 .
  
  lld:C1275122 a ncit:C7057 .
  
  dgn-gda:DGN5ca174e0af98d695fcd3321f6ce93ea2 sio:SIO_000628 miriam-gene:1021, lld:C1275122;
    a sio:SIO_001121 .
}

dgn-np:NP181412.RAXv6aXggSt1DPdKl_nMPcHkwDO7W-Y6aCPVfmEIRCT00130_provenance {
  dgn-np:NP181412.RAXv6aXggSt1DPdKl_nMPcHkwDO7W-Y6aCPVfmEIRCT00130_assertion dcterms:description
      "[The ESCC and EAC genomes showed some copy number abnormalities with similar frequencies (eg, CDKN2A, EGFR, KRAS, MYC, CDK6, MET) but also many copy number abnormalities with different frequencies between histologic types, most of which were amplification events.]. 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:22450065;
    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:NP181412.RAXv6aXggSt1DPdKl_nMPcHkwDO7W-Y6aCPVfmEIRCT00130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:38+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" .
}