@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP196522.RABEXghuNM173TjJlBT56bTkl_v7jcLi33p1WDYaZQebM> .
@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 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:NP196522.RABEXghuNM173TjJlBT56bTkl_v7jcLi33p1WDYaZQebM130_head {
   this: np:hasAssertion dgn-np:NP196522.RABEXghuNM173TjJlBT56bTkl_v7jcLi33p1WDYaZQebM130_assertion ;
    np:hasProvenance dgn-np:NP196522.RABEXghuNM173TjJlBT56bTkl_v7jcLi33p1WDYaZQebM130_provenance ;
    np:hasPublicationInfo dgn-np:NP196522.RABEXghuNM173TjJlBT56bTkl_v7jcLi33p1WDYaZQebM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP196522.RABEXghuNM173TjJlBT56bTkl_v7jcLi33p1WDYaZQebM130_assertion a np:Assertion .
  dgn-np:NP196522.RABEXghuNM173TjJlBT56bTkl_v7jcLi33p1WDYaZQebM130_provenance a np:Provenance .
  dgn-np:NP196522.RABEXghuNM173TjJlBT56bTkl_v7jcLi33p1WDYaZQebM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP196522.RABEXghuNM173TjJlBT56bTkl_v7jcLi33p1WDYaZQebM130_assertion {
   miriam-gene:1029 a ncit:C16612 .
  lld:C2939419 a ncit:C7057 .
  dgn-gda:DGN80aba2528b90565abb7f703232d5d6fb sio:SIO_000628 miriam-gene:1029 , lld:C2939419 ;
    a sio:SIO_001121 .
}
dgn-np:NP196522.RABEXghuNM173TjJlBT56bTkl_v7jcLi33p1WDYaZQebM130_provenance {
   dgn-np:NP196522.RABEXghuNM173TjJlBT56bTkl_v7jcLi33p1WDYaZQebM130_assertion dct: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:NP196522.RABEXghuNM173TjJlBT56bTkl_v7jcLi33p1WDYaZQebM130_publicationInfo {
   this: dct:created "2014-10-02T12:33:48+02:00"^^xsd:dateTime ;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dct:rightsHolder dgn-void:IBIGroup ;
    dct:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy orcid:0000-0001-5999-6269 , orcid:0000-0002-7534-7661 , orcid:0000-0002-9383-528X , orcid:0000-0003-0169-8159 , orcid:0000-0003-1244-7654 ;
    pav:createdBy orcid:0000-0003-0169-8159 ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}