@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP582736.RAlxJivrI5b8Ji0kiICTp99kD_u49yJI17tzBrJgkVAxQ> .
@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:NP582736.RAlxJivrI5b8Ji0kiICTp99kD_u49yJI17tzBrJgkVAxQ130_head {
  this: np:hasAssertion dgn-np:NP582736.RAlxJivrI5b8Ji0kiICTp99kD_u49yJI17tzBrJgkVAxQ130_assertion;
    np:hasProvenance dgn-np:NP582736.RAlxJivrI5b8Ji0kiICTp99kD_u49yJI17tzBrJgkVAxQ130_provenance;
    np:hasPublicationInfo dgn-np:NP582736.RAlxJivrI5b8Ji0kiICTp99kD_u49yJI17tzBrJgkVAxQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP582736.RAlxJivrI5b8Ji0kiICTp99kD_u49yJI17tzBrJgkVAxQ130_assertion a np:Assertion .
  
  dgn-np:NP582736.RAlxJivrI5b8Ji0kiICTp99kD_u49yJI17tzBrJgkVAxQ130_provenance a np:Provenance .
  
  dgn-np:NP582736.RAlxJivrI5b8Ji0kiICTp99kD_u49yJI17tzBrJgkVAxQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP582736.RAlxJivrI5b8Ji0kiICTp99kD_u49yJI17tzBrJgkVAxQ130_assertion {
  miriam-gene:4255 a ncit:C16612 .
  
  lld:C2939419 a ncit:C7057 .
  
  dgn-gda:DGN5c16f7d7f4ecb14eb2c7a0123e8f5429 sio:SIO_000628 miriam-gene:4255, lld:C2939419;
    a sio:SIO_001121 .
}

dgn-np:NP582736.RAlxJivrI5b8Ji0kiICTp99kD_u49yJI17tzBrJgkVAxQ130_provenance {
  dgn-np:NP582736.RAlxJivrI5b8Ji0kiICTp99kD_u49yJI17tzBrJgkVAxQ130_assertion dcterms:description
      "[Intratumor heterogeneity for expression of P16INK4a and MGMT may reflect intratumor heterogeneity for methylation patterns and thereby in general explain the moderate sensitivity of our marker panel for detection of metastases.]. 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:22266550;
    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:NP582736.RAlxJivrI5b8Ji0kiICTp99kD_u49yJI17tzBrJgkVAxQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:51+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" .
}