@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP294098.RAE5996XaYD3GcfwsUS_whBN3eZtePii-V6u76VcueJzc> .
@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:NP294098.RAE5996XaYD3GcfwsUS_whBN3eZtePii-V6u76VcueJzc130_head {
  this: np:hasAssertion dgn-np:NP294098.RAE5996XaYD3GcfwsUS_whBN3eZtePii-V6u76VcueJzc130_assertion;
    np:hasProvenance dgn-np:NP294098.RAE5996XaYD3GcfwsUS_whBN3eZtePii-V6u76VcueJzc130_provenance;
    np:hasPublicationInfo dgn-np:NP294098.RAE5996XaYD3GcfwsUS_whBN3eZtePii-V6u76VcueJzc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP294098.RAE5996XaYD3GcfwsUS_whBN3eZtePii-V6u76VcueJzc130_assertion a np:Assertion .
  
  dgn-np:NP294098.RAE5996XaYD3GcfwsUS_whBN3eZtePii-V6u76VcueJzc130_provenance a np:Provenance .
  
  dgn-np:NP294098.RAE5996XaYD3GcfwsUS_whBN3eZtePii-V6u76VcueJzc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP294098.RAE5996XaYD3GcfwsUS_whBN3eZtePii-V6u76VcueJzc130_assertion {
  miriam-gene:7750 a ncit:C16612 .
  
  lld:C2827362 a ncit:C7057 .
  
  dgn-gda:DGNdf10504cda406158bbb04d4ccbce6af5 sio:SIO_000628 miriam-gene:7750, lld:C2827362;
    a sio:SIO_001121 .
}

dgn-np:NP294098.RAE5996XaYD3GcfwsUS_whBN3eZtePii-V6u76VcueJzc130_provenance {
  dgn-np:NP294098.RAE5996XaYD3GcfwsUS_whBN3eZtePii-V6u76VcueJzc130_assertion dcterms:description
      "[The t(8;13)(p11;q12) is the most common translocation associated with the 8p11 myeloproliferative syndrome and results in an identical mRNA fusion between ZNF198 at 13q12 and FGFR1 at 8p11 in all cases thus far reported.]. 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:9889006;
    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:NP294098.RAE5996XaYD3GcfwsUS_whBN3eZtePii-V6u76VcueJzc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:47+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" .
}