@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP421070.RAaN1zibxP1OjoCgphfg1-JvR3Ul-LmCpCYfObKGtKqIY> .
@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:NP421070.RAaN1zibxP1OjoCgphfg1-JvR3Ul-LmCpCYfObKGtKqIY130_head {
  this: np:hasAssertion dgn-np:NP421070.RAaN1zibxP1OjoCgphfg1-JvR3Ul-LmCpCYfObKGtKqIY130_assertion;
    np:hasProvenance dgn-np:NP421070.RAaN1zibxP1OjoCgphfg1-JvR3Ul-LmCpCYfObKGtKqIY130_provenance;
    np:hasPublicationInfo dgn-np:NP421070.RAaN1zibxP1OjoCgphfg1-JvR3Ul-LmCpCYfObKGtKqIY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP421070.RAaN1zibxP1OjoCgphfg1-JvR3Ul-LmCpCYfObKGtKqIY130_assertion a np:Assertion .
  
  dgn-np:NP421070.RAaN1zibxP1OjoCgphfg1-JvR3Ul-LmCpCYfObKGtKqIY130_provenance a np:Provenance .
  
  dgn-np:NP421070.RAaN1zibxP1OjoCgphfg1-JvR3Ul-LmCpCYfObKGtKqIY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP421070.RAaN1zibxP1OjoCgphfg1-JvR3Ul-LmCpCYfObKGtKqIY130_assertion {
  miriam-gene:1788 a ncit:C16612 .
  
  lld:C0026986 a ncit:C7057 .
  
  dgn-gda:DGN3143d9dcd5a4135ae98eff0049276e7c sio:SIO_000628 miriam-gene:1788, lld:C0026986;
    a sio:SIO_001121 .
}

dgn-np:NP421070.RAaN1zibxP1OjoCgphfg1-JvR3Ul-LmCpCYfObKGtKqIY130_provenance {
  dgn-np:NP421070.RAaN1zibxP1OjoCgphfg1-JvR3Ul-LmCpCYfObKGtKqIY130_assertion dcterms:description
      "[We sequenced all coding exons of DNMT3A using DNA from bone marrow and paired normal cells from 150 patients with MDS and identified 13 heterozygous mutations with predicted translational consequences in 12/150 patients (8.0%).]. 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:21415852;
    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:NP421070.RAaN1zibxP1OjoCgphfg1-JvR3Ul-LmCpCYfObKGtKqIY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:10+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" .
}