@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP523402.RATMlNZHdaUn3CLRsd1ajVTNmJr80QHqeNR0l35sVZYx4> .
@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:NP523402.RATMlNZHdaUn3CLRsd1ajVTNmJr80QHqeNR0l35sVZYx4130_head {
  this: np:hasAssertion dgn-np:NP523402.RATMlNZHdaUn3CLRsd1ajVTNmJr80QHqeNR0l35sVZYx4130_assertion;
    np:hasProvenance dgn-np:NP523402.RATMlNZHdaUn3CLRsd1ajVTNmJr80QHqeNR0l35sVZYx4130_provenance;
    np:hasPublicationInfo dgn-np:NP523402.RATMlNZHdaUn3CLRsd1ajVTNmJr80QHqeNR0l35sVZYx4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP523402.RATMlNZHdaUn3CLRsd1ajVTNmJr80QHqeNR0l35sVZYx4130_assertion a np:Assertion .
  
  dgn-np:NP523402.RATMlNZHdaUn3CLRsd1ajVTNmJr80QHqeNR0l35sVZYx4130_provenance a np:Provenance .
  
  dgn-np:NP523402.RATMlNZHdaUn3CLRsd1ajVTNmJr80QHqeNR0l35sVZYx4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP523402.RATMlNZHdaUn3CLRsd1ajVTNmJr80QHqeNR0l35sVZYx4130_assertion {
  miriam-gene:2811 a ncit:C16612 .
  
  lld:C2586012 a ncit:C7057 .
  
  dgn-gda:DGN3650878b0970a8f6a6f831c1f9ec7352 sio:SIO_000628 miriam-gene:2811, lld:C2586012;
    a sio:SIO_001121 .
}

dgn-np:NP523402.RATMlNZHdaUn3CLRsd1ajVTNmJr80QHqeNR0l35sVZYx4130_provenance {
  dgn-np:NP523402.RATMlNZHdaUn3CLRsd1ajVTNmJr80QHqeNR0l35sVZYx4130_assertion dcterms:description
      "[To better understand the pathogenesis of thrombopoiesis in this hereditary thrombocytopenic disorder, we determined the percentage of reticulated platelets (RP), plasma glycocalicin (GC) and thrombopoietin (TPO) levels in 29 patients with CHMT, 23 patients with immune thrombocytopenic purpura (ITP), and 17 patients with thrombocytopenia secondary to decreased bone marrow megakaryocytes (hypoplasia).]. 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:10997880;
    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:NP523402.RATMlNZHdaUn3CLRsd1ajVTNmJr80QHqeNR0l35sVZYx4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:14+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" .
}