@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP75852.RAvLNs9xXg7S419exdTn4AuUC-S5htGNyLR9VXlBzGwB8> .
@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:NP75852.RAvLNs9xXg7S419exdTn4AuUC-S5htGNyLR9VXlBzGwB8130_head {
  this: np:hasAssertion dgn-np:NP75852.RAvLNs9xXg7S419exdTn4AuUC-S5htGNyLR9VXlBzGwB8130_assertion;
    np:hasProvenance dgn-np:NP75852.RAvLNs9xXg7S419exdTn4AuUC-S5htGNyLR9VXlBzGwB8130_provenance;
    np:hasPublicationInfo dgn-np:NP75852.RAvLNs9xXg7S419exdTn4AuUC-S5htGNyLR9VXlBzGwB8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP75852.RAvLNs9xXg7S419exdTn4AuUC-S5htGNyLR9VXlBzGwB8130_assertion a np:Assertion .
  
  dgn-np:NP75852.RAvLNs9xXg7S419exdTn4AuUC-S5htGNyLR9VXlBzGwB8130_provenance a np:Provenance .
  
  dgn-np:NP75852.RAvLNs9xXg7S419exdTn4AuUC-S5htGNyLR9VXlBzGwB8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP75852.RAvLNs9xXg7S419exdTn4AuUC-S5htGNyLR9VXlBzGwB8130_assertion {
  miriam-gene:1789 a ncit:C16612 .
  
  lld:C0043117 a ncit:C7057 .
  
  dgn-gda:DGN50ae901eb61bfe571da85165f0462fd2 sio:SIO_000628 miriam-gene:1789, lld:C0043117;
    a sio:SIO_001122 .
}

dgn-np:NP75852.RAvLNs9xXg7S419exdTn4AuUC-S5htGNyLR9VXlBzGwB8130_provenance {
  dgn-np:NP75852.RAvLNs9xXg7S419exdTn4AuUC-S5htGNyLR9VXlBzGwB8130_assertion dcterms:description
      "[The purpose of this study was to investigate the association between the single nucleotide polymorphism (SNP) in promoter of the DNMT3B gene and the risk for development of idiopathic thrombocytopenic purpura (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:18437543;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP75852.RAvLNs9xXg7S419exdTn4AuUC-S5htGNyLR9VXlBzGwB8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:37+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" .
}