@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP414164.RAgJSn6q7fpGXl2MTkOhgztEpkcJmclkw3EynpnUp9H4k> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP414164.RAgJSn6q7fpGXl2MTkOhgztEpkcJmclkw3EynpnUp9H4k130_head {
  this: np:hasAssertion dgn-np:NP414164.RAgJSn6q7fpGXl2MTkOhgztEpkcJmclkw3EynpnUp9H4k130_assertion;
    np:hasProvenance dgn-np:NP414164.RAgJSn6q7fpGXl2MTkOhgztEpkcJmclkw3EynpnUp9H4k130_provenance;
    np:hasPublicationInfo dgn-np:NP414164.RAgJSn6q7fpGXl2MTkOhgztEpkcJmclkw3EynpnUp9H4k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP414164.RAgJSn6q7fpGXl2MTkOhgztEpkcJmclkw3EynpnUp9H4k130_assertion a np:Assertion .
  
  dgn-np:NP414164.RAgJSn6q7fpGXl2MTkOhgztEpkcJmclkw3EynpnUp9H4k130_provenance a np:Provenance .
  
  dgn-np:NP414164.RAgJSn6q7fpGXl2MTkOhgztEpkcJmclkw3EynpnUp9H4k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP414164.RAgJSn6q7fpGXl2MTkOhgztEpkcJmclkw3EynpnUp9H4k130_assertion {
  miriam-gene:2521 a ncit:C16612 .
  
  lld:C0206634 a ncit:C7057 .
  
  dgn-gda:DGNb532632c0fb50cda55b25a95199f0718 sio:SIO_000628 miriam-gene:2521, lld:C0206634;
    a sio:SIO_001121 .
}

dgn-np:NP414164.RAgJSn6q7fpGXl2MTkOhgztEpkcJmclkw3EynpnUp9H4k130_provenance {
  dgn-np:NP414164.RAgJSn6q7fpGXl2MTkOhgztEpkcJmclkw3EynpnUp9H4k130_assertion dcterms:description
      "[Our results suggest that characteristic sequence motifs located at the FUS, EWS and CHOP breakpoint regions, including Alu and palindromic oligomer sequences, are involved in the mechanisms creating chromosomal translocations in MLS.]. 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:18752119;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP414164.RAgJSn6q7fpGXl2MTkOhgztEpkcJmclkw3EynpnUp9H4k130_publicationInfo {
  this: dcterms:created "2015-08-25T14:41:41+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}