@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP325794.RAQw3XiwWfzvo1RzLM9Ta9ZJQXcvMvvhKLEPSwk3Xz-xc> .
@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:NP325794.RAQw3XiwWfzvo1RzLM9Ta9ZJQXcvMvvhKLEPSwk3Xz-xc130_head {
  this: np:hasAssertion dgn-np:NP325794.RAQw3XiwWfzvo1RzLM9Ta9ZJQXcvMvvhKLEPSwk3Xz-xc130_assertion ;
    np:hasProvenance dgn-np:NP325794.RAQw3XiwWfzvo1RzLM9Ta9ZJQXcvMvvhKLEPSwk3Xz-xc130_provenance ;
    np:hasPublicationInfo dgn-np:NP325794.RAQw3XiwWfzvo1RzLM9Ta9ZJQXcvMvvhKLEPSwk3Xz-xc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP325794.RAQw3XiwWfzvo1RzLM9Ta9ZJQXcvMvvhKLEPSwk3Xz-xc130_assertion a np:Assertion .
  dgn-np:NP325794.RAQw3XiwWfzvo1RzLM9Ta9ZJQXcvMvvhKLEPSwk3Xz-xc130_provenance a np:Provenance .
  dgn-np:NP325794.RAQw3XiwWfzvo1RzLM9Ta9ZJQXcvMvvhKLEPSwk3Xz-xc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP325794.RAQw3XiwWfzvo1RzLM9Ta9ZJQXcvMvvhKLEPSwk3Xz-xc130_assertion {
  miriam-gene:5914 a ncit:C16612 .
  lld:C1859592 a ncit:C7057 .
  dgn-gda:DGN2c7306a500477682de747db11f2f15d6 sio:SIO_000628 miriam-gene:5914 , lld:C1859592 ;
    a sio:SIO_001121 .
}
dgn-np:NP325794.RAQw3XiwWfzvo1RzLM9Ta9ZJQXcvMvvhKLEPSwk3Xz-xc130_provenance {
  dgn-np:NP325794.RAQw3XiwWfzvo1RzLM9Ta9ZJQXcvMvvhKLEPSwk3Xz-xc130_assertion dcterms:description "[These data, along with previous reports of rare variant translocations in APL, indicate that while dysregulation of RARA by gene fusion may be essential for the APL phenotype, the particular fusion partner may determine clinicopathological aspects, including presentation, response to treatment with all-trans retinoic acid (ATRA), and prognosis.]. 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:8618456 ;
    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:NP325794.RAQw3XiwWfzvo1RzLM9Ta9ZJQXcvMvvhKLEPSwk3Xz-xc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:10+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" .
}