@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP549790.RAD73s54849bFQNatOCtTyUf0NClxb6X-3UFJ3h-TG4GI> .
@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:NP549790.RAD73s54849bFQNatOCtTyUf0NClxb6X-3UFJ3h-TG4GI130_head {
  this: np:hasAssertion dgn-np:NP549790.RAD73s54849bFQNatOCtTyUf0NClxb6X-3UFJ3h-TG4GI130_assertion;
    np:hasProvenance dgn-np:NP549790.RAD73s54849bFQNatOCtTyUf0NClxb6X-3UFJ3h-TG4GI130_provenance;
    np:hasPublicationInfo dgn-np:NP549790.RAD73s54849bFQNatOCtTyUf0NClxb6X-3UFJ3h-TG4GI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP549790.RAD73s54849bFQNatOCtTyUf0NClxb6X-3UFJ3h-TG4GI130_assertion a np:Assertion .
  
  dgn-np:NP549790.RAD73s54849bFQNatOCtTyUf0NClxb6X-3UFJ3h-TG4GI130_provenance a np:Provenance .
  
  dgn-np:NP549790.RAD73s54849bFQNatOCtTyUf0NClxb6X-3UFJ3h-TG4GI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP549790.RAD73s54849bFQNatOCtTyUf0NClxb6X-3UFJ3h-TG4GI130_assertion {
  miriam-gene:112399 a ncit:C16612 .
  
  lld:C0024419 a ncit:C7057 .
  
  dgn-gda:DGN71d043800a7b65c9a676292be05e6019 sio:SIO_000628 miriam-gene:112399, lld:C0024419;
    a sio:SIO_001121 .
}

dgn-np:NP549790.RAD73s54849bFQNatOCtTyUf0NClxb6X-3UFJ3h-TG4GI130_provenance {
  dgn-np:NP549790.RAD73s54849bFQNatOCtTyUf0NClxb6X-3UFJ3h-TG4GI130_assertion dcterms:description
      "[Analyses of a well-characterised series of cases of plasma cell dyscrasias, including multiple myeloma (MM), Waldenström's macroglobulinaemia (WM) and monoclonal gammopathy of undetermined significance (MGUS) surprisingly demonstrated that the CpG island of EGLN3, and not EGLN1, is frequently methylated in these disorders.]. 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:19737309;
    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:NP549790.RAD73s54849bFQNatOCtTyUf0NClxb6X-3UFJ3h-TG4GI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:31+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" .
}