@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP641727.RAPflqfPQ0c3lqecNAXbvyeiU_cPM6iWwkDKPvPU-MjLA> .
@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:NP641727.RAPflqfPQ0c3lqecNAXbvyeiU_cPM6iWwkDKPvPU-MjLA130_head {
  this: np:hasAssertion dgn-np:NP641727.RAPflqfPQ0c3lqecNAXbvyeiU_cPM6iWwkDKPvPU-MjLA130_assertion ;
    np:hasProvenance dgn-np:NP641727.RAPflqfPQ0c3lqecNAXbvyeiU_cPM6iWwkDKPvPU-MjLA130_provenance ;
    np:hasPublicationInfo dgn-np:NP641727.RAPflqfPQ0c3lqecNAXbvyeiU_cPM6iWwkDKPvPU-MjLA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP641727.RAPflqfPQ0c3lqecNAXbvyeiU_cPM6iWwkDKPvPU-MjLA130_assertion a np:Assertion .
  dgn-np:NP641727.RAPflqfPQ0c3lqecNAXbvyeiU_cPM6iWwkDKPvPU-MjLA130_provenance a np:Provenance .
  dgn-np:NP641727.RAPflqfPQ0c3lqecNAXbvyeiU_cPM6iWwkDKPvPU-MjLA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP641727.RAPflqfPQ0c3lqecNAXbvyeiU_cPM6iWwkDKPvPU-MjLA130_assertion {
  miriam-gene:2187 a ncit:C16612 .
  lld:C1879321 a ncit:C7057 .
  dgn-gda:DGN25e3e5a087f18ebf0f3007014de9e2aa sio:SIO_000628 miriam-gene:2187 , lld:C1879321 ;
    a sio:SIO_001121 .
}
dgn-np:NP641727.RAPflqfPQ0c3lqecNAXbvyeiU_cPM6iWwkDKPvPU-MjLA130_provenance {
  dgn-np:NP641727.RAPflqfPQ0c3lqecNAXbvyeiU_cPM6iWwkDKPvPU-MjLA130_assertion dcterms:description "[Certain cytogenetic changes were closely associated with French-American-British (FAB) morphology, age, and outcome: t(8;21) (closely associated with FAB M2), t(15;17) (associated with FAB M3), and abn 16q22 (associated with FAB M4EOS) tended to occur in younger patients and were associated with favorable outcomes in terms of both CR rate and long-term disease-free survival.]. 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:2910364 ;
    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:NP641727.RAPflqfPQ0c3lqecNAXbvyeiU_cPM6iWwkDKPvPU-MjLA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:27+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" .
}