@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP358120.RArW0LiINA21jfEycYqSSydAV_mjU6GHz6_li_Rh-kWRc> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP358120.RArW0LiINA21jfEycYqSSydAV_mjU6GHz6_li_Rh-kWRc130_head {
  this: np:hasAssertion dgn-np:NP358120.RArW0LiINA21jfEycYqSSydAV_mjU6GHz6_li_Rh-kWRc130_assertion;
    np:hasProvenance dgn-np:NP358120.RArW0LiINA21jfEycYqSSydAV_mjU6GHz6_li_Rh-kWRc130_provenance;
    np:hasPublicationInfo dgn-np:NP358120.RArW0LiINA21jfEycYqSSydAV_mjU6GHz6_li_Rh-kWRc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP358120.RArW0LiINA21jfEycYqSSydAV_mjU6GHz6_li_Rh-kWRc130_assertion a np:Assertion .
  
  dgn-np:NP358120.RArW0LiINA21jfEycYqSSydAV_mjU6GHz6_li_Rh-kWRc130_provenance a np:Provenance .
  
  dgn-np:NP358120.RArW0LiINA21jfEycYqSSydAV_mjU6GHz6_li_Rh-kWRc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP358120.RArW0LiINA21jfEycYqSSydAV_mjU6GHz6_li_Rh-kWRc130_assertion {
  miriam-gene:1789 a ncit:C16612 .
  
  lld:C1306459 a ncit:C7057 .
  
  dgn-gda:DGN36e6f1048924eb25416794d55fef4408 sio:SIO_000628 miriam-gene:1789, lld:C1306459;
    a sio:SIO_001121 .
}

dgn-np:NP358120.RArW0LiINA21jfEycYqSSydAV_mjU6GHz6_li_Rh-kWRc130_provenance {
  dgn-np:NP358120.RArW0LiINA21jfEycYqSSydAV_mjU6GHz6_li_Rh-kWRc130_assertion dcterms:description
      "[Indeed, the de novo methyltransferase 3B (DNMT3B) has been recently found to be mutated in several types of cancer and in the immunodeficiency, centromeric region instability and facial anomalies syndrome (ICF), in which these mutations could be related to the loss of global DNA methylation.]. 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:23474979;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP358120.RArW0LiINA21jfEycYqSSydAV_mjU6GHz6_li_Rh-kWRc130_publicationInfo {
  this: dcterms:created "2015-08-25T14:41:06+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}