@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP275726.RAdyzTNmKJe2UeYhFIa2ydgk5giTyrH7y4zxxKvRysOwQ> .
@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:NP275726.RAdyzTNmKJe2UeYhFIa2ydgk5giTyrH7y4zxxKvRysOwQ130_head {
  this: np:hasAssertion dgn-np:NP275726.RAdyzTNmKJe2UeYhFIa2ydgk5giTyrH7y4zxxKvRysOwQ130_assertion;
    np:hasProvenance dgn-np:NP275726.RAdyzTNmKJe2UeYhFIa2ydgk5giTyrH7y4zxxKvRysOwQ130_provenance;
    np:hasPublicationInfo dgn-np:NP275726.RAdyzTNmKJe2UeYhFIa2ydgk5giTyrH7y4zxxKvRysOwQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP275726.RAdyzTNmKJe2UeYhFIa2ydgk5giTyrH7y4zxxKvRysOwQ130_assertion a np:Assertion .
  
  dgn-np:NP275726.RAdyzTNmKJe2UeYhFIa2ydgk5giTyrH7y4zxxKvRysOwQ130_provenance a np:Provenance .
  
  dgn-np:NP275726.RAdyzTNmKJe2UeYhFIa2ydgk5giTyrH7y4zxxKvRysOwQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP275726.RAdyzTNmKJe2UeYhFIa2ydgk5giTyrH7y4zxxKvRysOwQ130_assertion {
  miriam-gene:4363 a ncit:C16612 .
  
  lld:C1961102 a ncit:C7057 .
  
  dgn-gda:DGNd3c6735d5e688ede81c8f44b8435f9f4 sio:SIO_000628 miriam-gene:4363, lld:C1961102;
    a sio:SIO_001121 .
}

dgn-np:NP275726.RAdyzTNmKJe2UeYhFIa2ydgk5giTyrH7y4zxxKvRysOwQ130_provenance {
  dgn-np:NP275726.RAdyzTNmKJe2UeYhFIa2ydgk5giTyrH7y4zxxKvRysOwQ130_assertion dcterms:description
      "[The findings suggest that high MRP1 expression was associated with poor clinical outcome and was correlated with the M5 subtype and poor cytogenetic subgroups among AML patients but not among ALL patients.]. 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:18711657;
    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:NP275726.RAdyzTNmKJe2UeYhFIa2ydgk5giTyrH7y4zxxKvRysOwQ130_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" .
}