@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP276041.RAQUwXjLNhEwSBL327sYifa3HAfu1CczsJuFhE69irTGk> .
@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:NP276041.RAQUwXjLNhEwSBL327sYifa3HAfu1CczsJuFhE69irTGk130_head {
  this: np:hasAssertion dgn-np:NP276041.RAQUwXjLNhEwSBL327sYifa3HAfu1CczsJuFhE69irTGk130_assertion;
    np:hasProvenance dgn-np:NP276041.RAQUwXjLNhEwSBL327sYifa3HAfu1CczsJuFhE69irTGk130_provenance;
    np:hasPublicationInfo dgn-np:NP276041.RAQUwXjLNhEwSBL327sYifa3HAfu1CczsJuFhE69irTGk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP276041.RAQUwXjLNhEwSBL327sYifa3HAfu1CczsJuFhE69irTGk130_assertion a np:Assertion .
  
  dgn-np:NP276041.RAQUwXjLNhEwSBL327sYifa3HAfu1CczsJuFhE69irTGk130_provenance a np:Provenance .
  
  dgn-np:NP276041.RAQUwXjLNhEwSBL327sYifa3HAfu1CczsJuFhE69irTGk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP276041.RAQUwXjLNhEwSBL327sYifa3HAfu1CczsJuFhE69irTGk130_assertion {
  miriam-gene:23326 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGN156febf71d5563a9da6580cc58ab81e2 sio:SIO_000628 miriam-gene:23326, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP276041.RAQUwXjLNhEwSBL327sYifa3HAfu1CczsJuFhE69irTGk130_provenance {
  dgn-np:NP276041.RAQUwXjLNhEwSBL327sYifa3HAfu1CczsJuFhE69irTGk130_assertion dcterms:description
      "[The simultaneous targeting of USP22, and its downstream signal transduction molecules seem highly informative in stratification of the cancer into subgroups with distinct likelihood of therapy failure, which contribute to make decision process regarding the individualized therapy selection and optimization.]. 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:22717106;
    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:NP276041.RAQUwXjLNhEwSBL327sYifa3HAfu1CczsJuFhE69irTGk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:35+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" .
}