@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP157761.RAQkEO6-iE2mKDYs3VIPJi_wsuWPRuZIZbw8RLGp69jMQ> .
@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:NP157761.RAQkEO6-iE2mKDYs3VIPJi_wsuWPRuZIZbw8RLGp69jMQ130_head {
  this: np:hasAssertion dgn-np:NP157761.RAQkEO6-iE2mKDYs3VIPJi_wsuWPRuZIZbw8RLGp69jMQ130_assertion;
    np:hasProvenance dgn-np:NP157761.RAQkEO6-iE2mKDYs3VIPJi_wsuWPRuZIZbw8RLGp69jMQ130_provenance;
    np:hasPublicationInfo dgn-np:NP157761.RAQkEO6-iE2mKDYs3VIPJi_wsuWPRuZIZbw8RLGp69jMQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP157761.RAQkEO6-iE2mKDYs3VIPJi_wsuWPRuZIZbw8RLGp69jMQ130_assertion a np:Assertion .
  
  dgn-np:NP157761.RAQkEO6-iE2mKDYs3VIPJi_wsuWPRuZIZbw8RLGp69jMQ130_provenance a np:Provenance .
  
  dgn-np:NP157761.RAQkEO6-iE2mKDYs3VIPJi_wsuWPRuZIZbw8RLGp69jMQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP157761.RAQkEO6-iE2mKDYs3VIPJi_wsuWPRuZIZbw8RLGp69jMQ130_assertion {
  miriam-gene:3265 a ncit:C16612 .
  
  lld:C0023418 a ncit:C7057 .
  
  dgn-gda:DGN586f6bd416cd6e45d83ccb163390ccc5 sio:SIO_000628 miriam-gene:3265, lld:C0023418;
    a sio:SIO_001121 .
}

dgn-np:NP157761.RAQkEO6-iE2mKDYs3VIPJi_wsuWPRuZIZbw8RLGp69jMQ130_provenance {
  dgn-np:NP157761.RAQkEO6-iE2mKDYs3VIPJi_wsuWPRuZIZbw8RLGp69jMQ130_assertion dcterms:description
      "[Because the INS gene, which was also translocated, is probably located proximal to HRAS1 on chromosome 11p, it is unlikely that HRAS1 was near the chromosome 11 breakpoint or involved in this leukaemia.]. 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:2713271;
    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:NP157761.RAQkEO6-iE2mKDYs3VIPJi_wsuWPRuZIZbw8RLGp69jMQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:25+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" .
}