@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP586037.RAPIewyKcXBJRKHTbujSFzLZRj2LMyVQSthvaI3Dy9EsU> .
@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:NP586037.RAPIewyKcXBJRKHTbujSFzLZRj2LMyVQSthvaI3Dy9EsU130_head {
  this: np:hasAssertion dgn-np:NP586037.RAPIewyKcXBJRKHTbujSFzLZRj2LMyVQSthvaI3Dy9EsU130_assertion;
    np:hasProvenance dgn-np:NP586037.RAPIewyKcXBJRKHTbujSFzLZRj2LMyVQSthvaI3Dy9EsU130_provenance;
    np:hasPublicationInfo dgn-np:NP586037.RAPIewyKcXBJRKHTbujSFzLZRj2LMyVQSthvaI3Dy9EsU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP586037.RAPIewyKcXBJRKHTbujSFzLZRj2LMyVQSthvaI3Dy9EsU130_assertion a np:Assertion .
  
  dgn-np:NP586037.RAPIewyKcXBJRKHTbujSFzLZRj2LMyVQSthvaI3Dy9EsU130_provenance a np:Provenance .
  
  dgn-np:NP586037.RAPIewyKcXBJRKHTbujSFzLZRj2LMyVQSthvaI3Dy9EsU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP586037.RAPIewyKcXBJRKHTbujSFzLZRj2LMyVQSthvaI3Dy9EsU130_assertion {
  miriam-gene:7490 a ncit:C16612 .
  
  lld:C0002893 a ncit:C7057 .
  
  dgn-gda:DGNb9e8a2718d39e15a9b797b96e8cf70f5 sio:SIO_000628 miriam-gene:7490, lld:C0002893;
    a sio:SIO_001121 .
}

dgn-np:NP586037.RAPIewyKcXBJRKHTbujSFzLZRj2LMyVQSthvaI3Dy9EsU130_provenance {
  dgn-np:NP586037.RAPIewyKcXBJRKHTbujSFzLZRj2LMyVQSthvaI3Dy9EsU130_assertion dcterms:description
      "[An increase of all three WT1 messages in high-grade MDS and acute leukemia was observed as compared with the normal control, whereas there was no significant difference in WT1 message between AA and RA, suggesting that WT1 message is not a good tool to discriminate AA and RA.]. 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:17803653;
    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:NP586037.RAPIewyKcXBJRKHTbujSFzLZRj2LMyVQSthvaI3Dy9EsU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:53+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" .
}