@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP656743.RArqMoTmZAJReoIDX1zCNWv_uQBea_KgtibH9HniGrl3A> .
@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:NP656743.RArqMoTmZAJReoIDX1zCNWv_uQBea_KgtibH9HniGrl3A130_head {
  this: np:hasAssertion dgn-np:NP656743.RArqMoTmZAJReoIDX1zCNWv_uQBea_KgtibH9HniGrl3A130_assertion;
    np:hasProvenance dgn-np:NP656743.RArqMoTmZAJReoIDX1zCNWv_uQBea_KgtibH9HniGrl3A130_provenance;
    np:hasPublicationInfo dgn-np:NP656743.RArqMoTmZAJReoIDX1zCNWv_uQBea_KgtibH9HniGrl3A130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP656743.RArqMoTmZAJReoIDX1zCNWv_uQBea_KgtibH9HniGrl3A130_assertion a np:Assertion .
  
  dgn-np:NP656743.RArqMoTmZAJReoIDX1zCNWv_uQBea_KgtibH9HniGrl3A130_provenance a np:Provenance .
  
  dgn-np:NP656743.RArqMoTmZAJReoIDX1zCNWv_uQBea_KgtibH9HniGrl3A130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP656743.RArqMoTmZAJReoIDX1zCNWv_uQBea_KgtibH9HniGrl3A130_assertion {
  miriam-gene:1788 a ncit:C16612 .
  
  lld:C0043117 a ncit:C7057 .
  
  dgn-gda:DGN1ea71bcc740fcc8635f523d5f773bb0e sio:SIO_000628 miriam-gene:1788, lld:C0043117;
    a sio:SIO_001121 .
}

dgn-np:NP656743.RArqMoTmZAJReoIDX1zCNWv_uQBea_KgtibH9HniGrl3A130_provenance {
  dgn-np:NP656743.RArqMoTmZAJReoIDX1zCNWv_uQBea_KgtibH9HniGrl3A130_assertion dcterms:description
      "[Conclusions:  Aberrant DNA methylation status reflected by decreased mRNA expression of DNMT3A and increased plasma SAH level may play an important role in the pathogenesis of ITP, although the precise underlying mechanisms still await further investigations, and extensive work in this field is clearly needed to provide novel therapeutic targets for ITP.]. 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:22321265;
    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:NP656743.RArqMoTmZAJReoIDX1zCNWv_uQBea_KgtibH9HniGrl3A130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:35+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" .
}