@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP877821.RAOC7fPPOJvLJm1-dCtT3uXjnkgXI3PGpfcNtMcehMsKA> .
@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:NP877821.RAOC7fPPOJvLJm1-dCtT3uXjnkgXI3PGpfcNtMcehMsKA130_head {
  this: np:hasAssertion dgn-np:NP877821.RAOC7fPPOJvLJm1-dCtT3uXjnkgXI3PGpfcNtMcehMsKA130_assertion;
    np:hasProvenance dgn-np:NP877821.RAOC7fPPOJvLJm1-dCtT3uXjnkgXI3PGpfcNtMcehMsKA130_provenance;
    np:hasPublicationInfo dgn-np:NP877821.RAOC7fPPOJvLJm1-dCtT3uXjnkgXI3PGpfcNtMcehMsKA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP877821.RAOC7fPPOJvLJm1-dCtT3uXjnkgXI3PGpfcNtMcehMsKA130_assertion a np:Assertion .
  
  dgn-np:NP877821.RAOC7fPPOJvLJm1-dCtT3uXjnkgXI3PGpfcNtMcehMsKA130_provenance a np:Provenance .
  
  dgn-np:NP877821.RAOC7fPPOJvLJm1-dCtT3uXjnkgXI3PGpfcNtMcehMsKA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP877821.RAOC7fPPOJvLJm1-dCtT3uXjnkgXI3PGpfcNtMcehMsKA130_assertion {
  miriam-gene:5066 a ncit:C16612 .
  
  lld:C1961099 a ncit:C7057 .
  
  dgn-gda:DGNd6a6126f932363175bd453c84853f532 sio:SIO_000628 miriam-gene:5066, lld:C1961099;
    a sio:SIO_001121 .
}

dgn-np:NP877821.RAOC7fPPOJvLJm1-dCtT3uXjnkgXI3PGpfcNtMcehMsKA130_provenance {
  dgn-np:NP877821.RAOC7fPPOJvLJm1-dCtT3uXjnkgXI3PGpfcNtMcehMsKA130_assertion dcterms:description
      "[Based on the hypothesis that microarrays might identify patients who fail therapy, we used the Affymetrix U133 Plus 2.0 chip and prediction analysis of microarrays (PAM) to profile 50 newly diagnosed patients who were treated in the Children's Oncology Group (COG) T-ALL Study 9404.]. 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:17495134;
    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:NP877821.RAOC7fPPOJvLJm1-dCtT3uXjnkgXI3PGpfcNtMcehMsKA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:56+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" .
}