@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP251943.RADX7S54L3N9gnk-j2wIDtkCYmdqL6G6CC4oyw7A3_mCU> .
@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:NP251943.RADX7S54L3N9gnk-j2wIDtkCYmdqL6G6CC4oyw7A3_mCU130_head {
  this: np:hasAssertion dgn-np:NP251943.RADX7S54L3N9gnk-j2wIDtkCYmdqL6G6CC4oyw7A3_mCU130_assertion;
    np:hasProvenance dgn-np:NP251943.RADX7S54L3N9gnk-j2wIDtkCYmdqL6G6CC4oyw7A3_mCU130_provenance;
    np:hasPublicationInfo dgn-np:NP251943.RADX7S54L3N9gnk-j2wIDtkCYmdqL6G6CC4oyw7A3_mCU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP251943.RADX7S54L3N9gnk-j2wIDtkCYmdqL6G6CC4oyw7A3_mCU130_assertion a np:Assertion .
  
  dgn-np:NP251943.RADX7S54L3N9gnk-j2wIDtkCYmdqL6G6CC4oyw7A3_mCU130_provenance a np:Provenance .
  
  dgn-np:NP251943.RADX7S54L3N9gnk-j2wIDtkCYmdqL6G6CC4oyw7A3_mCU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP251943.RADX7S54L3N9gnk-j2wIDtkCYmdqL6G6CC4oyw7A3_mCU130_assertion {
  miriam-gene:4928 a ncit:C16612 .
  
  lld:C0023418 a ncit:C7057 .
  
  dgn-gda:DGNd2cf2823cfa49e369d3a637708f4b2c8 sio:SIO_000628 miriam-gene:4928, lld:C0023418;
    a sio:SIO_001121 .
}

dgn-np:NP251943.RADX7S54L3N9gnk-j2wIDtkCYmdqL6G6CC4oyw7A3_mCU130_provenance {
  dgn-np:NP251943.RADX7S54L3N9gnk-j2wIDtkCYmdqL6G6CC4oyw7A3_mCU130_assertion dcterms:description
      "[Clinical findings are reviewed here, along with the findings of several in vivo and in vitro models have been employed to investigate the mechanisms by which NUP98 fusion genes contribute to the pathogenesis of leukemia.]. 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:15359631;
    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:NP251943.RADX7S54L3N9gnk-j2wIDtkCYmdqL6G6CC4oyw7A3_mCU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:20+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" .
}