@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP184570.RA2ixAyFVEndCSgCORCMOYsPA8zlaCuT4QVD4tVVb8Oak> .
@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:NP184570.RA2ixAyFVEndCSgCORCMOYsPA8zlaCuT4QVD4tVVb8Oak130_head {
  this: np:hasAssertion dgn-np:NP184570.RA2ixAyFVEndCSgCORCMOYsPA8zlaCuT4QVD4tVVb8Oak130_assertion;
    np:hasProvenance dgn-np:NP184570.RA2ixAyFVEndCSgCORCMOYsPA8zlaCuT4QVD4tVVb8Oak130_provenance;
    np:hasPublicationInfo dgn-np:NP184570.RA2ixAyFVEndCSgCORCMOYsPA8zlaCuT4QVD4tVVb8Oak130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP184570.RA2ixAyFVEndCSgCORCMOYsPA8zlaCuT4QVD4tVVb8Oak130_assertion a np:Assertion .
  
  dgn-np:NP184570.RA2ixAyFVEndCSgCORCMOYsPA8zlaCuT4QVD4tVVb8Oak130_provenance a np:Provenance .
  
  dgn-np:NP184570.RA2ixAyFVEndCSgCORCMOYsPA8zlaCuT4QVD4tVVb8Oak130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP184570.RA2ixAyFVEndCSgCORCMOYsPA8zlaCuT4QVD4tVVb8Oak130_assertion {
  miriam-gene:2768 a ncit:C16612 .
  
  lld:C0079744 a ncit:C7057 .
  
  dgn-gda:DGN2a0abfe51245537b8a285c786a01aee7 sio:SIO_000628 miriam-gene:2768, lld:C0079744;
    a sio:SIO_001121 .
}

dgn-np:NP184570.RA2ixAyFVEndCSgCORCMOYsPA8zlaCuT4QVD4tVVb8Oak130_provenance {
  dgn-np:NP184570.RA2ixAyFVEndCSgCORCMOYsPA8zlaCuT4QVD4tVVb8Oak130_assertion dcterms:description
      "[GEP categorization of COO is superior in defining prognostically and biologically distinct DLBCL subtypes, but current barriers to its widescale use include inaccessibility, cost, and lack of methodological standardization and prospective validation.]. 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:23086691;
    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:NP184570.RA2ixAyFVEndCSgCORCMOYsPA8zlaCuT4QVD4tVVb8Oak130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:40+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" .
}