@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP753434.RAc-XJSec1MdbqS5KzWNMp60DW49k4vQZrhnunZS1kXXw> .
@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:NP753434.RAc-XJSec1MdbqS5KzWNMp60DW49k4vQZrhnunZS1kXXw130_head {
  this: np:hasAssertion dgn-np:NP753434.RAc-XJSec1MdbqS5KzWNMp60DW49k4vQZrhnunZS1kXXw130_assertion ;
    np:hasProvenance dgn-np:NP753434.RAc-XJSec1MdbqS5KzWNMp60DW49k4vQZrhnunZS1kXXw130_provenance ;
    np:hasPublicationInfo dgn-np:NP753434.RAc-XJSec1MdbqS5KzWNMp60DW49k4vQZrhnunZS1kXXw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP753434.RAc-XJSec1MdbqS5KzWNMp60DW49k4vQZrhnunZS1kXXw130_assertion a np:Assertion .
  dgn-np:NP753434.RAc-XJSec1MdbqS5KzWNMp60DW49k4vQZrhnunZS1kXXw130_provenance a np:Provenance .
  dgn-np:NP753434.RAc-XJSec1MdbqS5KzWNMp60DW49k4vQZrhnunZS1kXXw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP753434.RAc-XJSec1MdbqS5KzWNMp60DW49k4vQZrhnunZS1kXXw130_assertion {
  miriam-gene:2056 a ncit:C16612 .
  lld:C0023434 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP753434.RAc-XJSec1MdbqS5KzWNMp60DW49k4vQZrhnunZS1kXXw130_provenance {
  dgn-np:NP753434.RAc-XJSec1MdbqS5KzWNMp60DW49k4vQZrhnunZS1kXXw130_assertion dcterms:description "[We genotyped the EPO rS1617640 SNP in 189 patients with MDS, 257 with acute myeloid leukemia (AML), 106 with acute lymphoblastic leukemia, 97 with chronic lymphocytic leukemia, 353 with chronic myeloid leukemia, and 95 healthy controls.]. 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:21078205 ;
    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:NP753434.RAc-XJSec1MdbqS5KzWNMp60DW49k4vQZrhnunZS1kXXw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:36+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 ;
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}