@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP263124.RAe5E29Yqj8FnszMKvkA1-kHoP4c3AcHQMEZK8sb4PtL4> .
@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:NP263124.RAe5E29Yqj8FnszMKvkA1-kHoP4c3AcHQMEZK8sb4PtL4130_head {
  this: np:hasAssertion dgn-np:NP263124.RAe5E29Yqj8FnszMKvkA1-kHoP4c3AcHQMEZK8sb4PtL4130_assertion;
    np:hasProvenance dgn-np:NP263124.RAe5E29Yqj8FnszMKvkA1-kHoP4c3AcHQMEZK8sb4PtL4130_provenance;
    np:hasPublicationInfo dgn-np:NP263124.RAe5E29Yqj8FnszMKvkA1-kHoP4c3AcHQMEZK8sb4PtL4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP263124.RAe5E29Yqj8FnszMKvkA1-kHoP4c3AcHQMEZK8sb4PtL4130_assertion a np:Assertion .
  
  dgn-np:NP263124.RAe5E29Yqj8FnszMKvkA1-kHoP4c3AcHQMEZK8sb4PtL4130_provenance a np:Provenance .
  
  dgn-np:NP263124.RAe5E29Yqj8FnszMKvkA1-kHoP4c3AcHQMEZK8sb4PtL4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP263124.RAe5E29Yqj8FnszMKvkA1-kHoP4c3AcHQMEZK8sb4PtL4130_assertion {
  miriam-gene:2187 a ncit:C16612 .
  
  lld:C0023418 a ncit:C7057 .
  
  dgn-gda:DGN266767829fbaa5bbad033af636755713 sio:SIO_000628 miriam-gene:2187, lld:C0023418;
    a sio:SIO_001121 .
}

dgn-np:NP263124.RAe5E29Yqj8FnszMKvkA1-kHoP4c3AcHQMEZK8sb4PtL4130_provenance {
  dgn-np:NP263124.RAe5E29Yqj8FnszMKvkA1-kHoP4c3AcHQMEZK8sb4PtL4130_assertion dcterms:description
      "[In 35 patients with normal karyotype and 16 patients with cytogenetic anomalies not presently associated with FAB subtypes the expected correlations of rather immature myeloid immunologic phenotypes with M1 and M2 morphology and CD14 expression in monoblastic leukemias was found.]. 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:1638477;
    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:NP263124.RAe5E29Yqj8FnszMKvkA1-kHoP4c3AcHQMEZK8sb4PtL4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:27+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" .
}