@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP910446.RAEq3JWitjXIyt3L55DGWof8ztzmex1gjPYr7Srs1ADhw> .
@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:NP910446.RAEq3JWitjXIyt3L55DGWof8ztzmex1gjPYr7Srs1ADhw130_head {
  this: np:hasAssertion dgn-np:NP910446.RAEq3JWitjXIyt3L55DGWof8ztzmex1gjPYr7Srs1ADhw130_assertion ;
    np:hasProvenance dgn-np:NP910446.RAEq3JWitjXIyt3L55DGWof8ztzmex1gjPYr7Srs1ADhw130_provenance ;
    np:hasPublicationInfo dgn-np:NP910446.RAEq3JWitjXIyt3L55DGWof8ztzmex1gjPYr7Srs1ADhw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP910446.RAEq3JWitjXIyt3L55DGWof8ztzmex1gjPYr7Srs1ADhw130_assertion a np:Assertion .
  dgn-np:NP910446.RAEq3JWitjXIyt3L55DGWof8ztzmex1gjPYr7Srs1ADhw130_provenance a np:Provenance .
  dgn-np:NP910446.RAEq3JWitjXIyt3L55DGWof8ztzmex1gjPYr7Srs1ADhw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP910446.RAEq3JWitjXIyt3L55DGWof8ztzmex1gjPYr7Srs1ADhw130_assertion {
  miriam-gene:1050 a ncit:C16612 .
  lld:C0023470 a ncit:C7057 .
  dgn-gda:DGN60cbef509879bcc07eb2ac5b0adddf3f sio:SIO_000628 miriam-gene:1050 , lld:C0023470 ;
    a sio:SIO_001121 .
}
dgn-np:NP910446.RAEq3JWitjXIyt3L55DGWof8ztzmex1gjPYr7Srs1ADhw130_provenance {
  dgn-np:NP910446.RAEq3JWitjXIyt3L55DGWof8ztzmex1gjPYr7Srs1ADhw130_assertion dcterms:description "[In order to strengthen this hypothesis, we have screened CEBPA for germline mutations in several families presenting aggregation of hematological malignancies (including chronic or acute, lymphoid or myeloid leukemias, Hodgkin's or non Hodgkin's lymphomas, and myeloproliferative or myelodysplastic syndromes) with or without solid tumours.]. 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:19731081 ;
    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:NP910446.RAEq3JWitjXIyt3L55DGWof8ztzmex1gjPYr7Srs1ADhw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:19+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 ;
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}