@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP60188.RA6GVx0An1h2LBhLk5zXVzdrowEo_78G80Zqtv_rZidq0> .
@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 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:NP60188.RA6GVx0An1h2LBhLk5zXVzdrowEo_78G80Zqtv_rZidq0130_head {
  this: np:hasAssertion dgn-np:NP60188.RA6GVx0An1h2LBhLk5zXVzdrowEo_78G80Zqtv_rZidq0130_assertion;
    np:hasProvenance dgn-np:NP60188.RA6GVx0An1h2LBhLk5zXVzdrowEo_78G80Zqtv_rZidq0130_provenance;
    np:hasPublicationInfo dgn-np:NP60188.RA6GVx0An1h2LBhLk5zXVzdrowEo_78G80Zqtv_rZidq0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP60188.RA6GVx0An1h2LBhLk5zXVzdrowEo_78G80Zqtv_rZidq0130_assertion a np:Assertion .
  
  dgn-np:NP60188.RA6GVx0An1h2LBhLk5zXVzdrowEo_78G80Zqtv_rZidq0130_provenance a np:Provenance .
  
  dgn-np:NP60188.RA6GVx0An1h2LBhLk5zXVzdrowEo_78G80Zqtv_rZidq0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP60188.RA6GVx0An1h2LBhLk5zXVzdrowEo_78G80Zqtv_rZidq0130_assertion {
  miriam-gene:1756 a ncit:C16612 .
  
  lld:C0026850 a ncit:C7057 .
  
  dgn-gda:DGNbdd1cdd83c1b132ff7d2be106d7595e3 sio:SIO_000628 miriam-gene:1756, lld:C0026850;
    a sio:SIO_001122 .
}

dgn-np:NP60188.RA6GVx0An1h2LBhLk5zXVzdrowEo_78G80Zqtv_rZidq0130_provenance {
  dgn-np:NP60188.RA6GVx0An1h2LBhLk5zXVzdrowEo_78G80Zqtv_rZidq0130_assertion dct:description
      "[Our results suggest that, although the presence and frequency of the two deletion hot spots may be similar in the three Asian populations analyzed, the distribution and frequency of deletions among the different exons can vary as a result of population-specific intronic sequences that predispose individuals to preferential deletion breakpoints.]. 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:12376747;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP60188.RA6GVx0An1h2LBhLk5zXVzdrowEo_78G80Zqtv_rZidq0130_publicationInfo {
  this: dct:created "2014-10-02T12:32:28+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}