@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP550349.RASQMyAS2OOExw498q6W9YvViCcbphjhyf8MfoLN3uNxE> .
@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:NP550349.RASQMyAS2OOExw498q6W9YvViCcbphjhyf8MfoLN3uNxE130_head {
  this: np:hasAssertion dgn-np:NP550349.RASQMyAS2OOExw498q6W9YvViCcbphjhyf8MfoLN3uNxE130_assertion;
    np:hasProvenance dgn-np:NP550349.RASQMyAS2OOExw498q6W9YvViCcbphjhyf8MfoLN3uNxE130_provenance;
    np:hasPublicationInfo dgn-np:NP550349.RASQMyAS2OOExw498q6W9YvViCcbphjhyf8MfoLN3uNxE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP550349.RASQMyAS2OOExw498q6W9YvViCcbphjhyf8MfoLN3uNxE130_assertion a np:Assertion .
  
  dgn-np:NP550349.RASQMyAS2OOExw498q6W9YvViCcbphjhyf8MfoLN3uNxE130_provenance a np:Provenance .
  
  dgn-np:NP550349.RASQMyAS2OOExw498q6W9YvViCcbphjhyf8MfoLN3uNxE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP550349.RASQMyAS2OOExw498q6W9YvViCcbphjhyf8MfoLN3uNxE130_assertion {
  miriam-gene:55672 a ncit:C16612 .
  
  lld:C0700095 a ncit:C7057 .
  
  dgn-gda:DGN2bdc356568e78fbd4f9008fbe3eeca5c sio:SIO_000628 miriam-gene:55672, lld:C0700095;
    a sio:SIO_001121 .
}

dgn-np:NP550349.RASQMyAS2OOExw498q6W9YvViCcbphjhyf8MfoLN3uNxE130_provenance {
  dgn-np:NP550349.RASQMyAS2OOExw498q6W9YvViCcbphjhyf8MfoLN3uNxE130_assertion dcterms:description
      "[Here, we describe the recent acquisition of the NBPF1 promoter from an unrelated gene, and remarkably, both the donor (EVI5) and acceptor (NBPF1) genes are disrupted by constitutional translocations in patients with neuroblastoma, suggesting a functional link between these genes and the disease.]. 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:19282512;
    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:NP550349.RASQMyAS2OOExw498q6W9YvViCcbphjhyf8MfoLN3uNxE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:32+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" .
}