@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP279546.RA5vWyz6LR1BZFSPIk1bKtlcIevA7vj98Fxffp_oGPjVw> .
@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:NP279546.RA5vWyz6LR1BZFSPIk1bKtlcIevA7vj98Fxffp_oGPjVw130_head {
  this: np:hasAssertion dgn-np:NP279546.RA5vWyz6LR1BZFSPIk1bKtlcIevA7vj98Fxffp_oGPjVw130_assertion;
    np:hasProvenance dgn-np:NP279546.RA5vWyz6LR1BZFSPIk1bKtlcIevA7vj98Fxffp_oGPjVw130_provenance;
    np:hasPublicationInfo dgn-np:NP279546.RA5vWyz6LR1BZFSPIk1bKtlcIevA7vj98Fxffp_oGPjVw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP279546.RA5vWyz6LR1BZFSPIk1bKtlcIevA7vj98Fxffp_oGPjVw130_assertion a np:Assertion .
  
  dgn-np:NP279546.RA5vWyz6LR1BZFSPIk1bKtlcIevA7vj98Fxffp_oGPjVw130_provenance a np:Provenance .
  
  dgn-np:NP279546.RA5vWyz6LR1BZFSPIk1bKtlcIevA7vj98Fxffp_oGPjVw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP279546.RA5vWyz6LR1BZFSPIk1bKtlcIevA7vj98Fxffp_oGPjVw130_assertion {
  miriam-gene:2120 a ncit:C16612 .
  
  lld:C0751606 a ncit:C7057 .
  
  dgn-gda:DGN6097fcf87a0e1d223ee9a034562cdf0c sio:SIO_000628 miriam-gene:2120, lld:C0751606;
    a sio:SIO_001121 .
}

dgn-np:NP279546.RA5vWyz6LR1BZFSPIk1bKtlcIevA7vj98Fxffp_oGPjVw130_provenance {
  dgn-np:NP279546.RA5vWyz6LR1BZFSPIk1bKtlcIevA7vj98Fxffp_oGPjVw130_assertion dcterms:description
      "[This study shows that multiplex-nested RT-PCR is an effective and accurate tool to identify ETV6 rearrangements in adult ALL, which provides some clues into the diagnosis and prognosis of ALL but also molecular markers for the detection of minimal residual disease in adult ALL.]. 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:22373549;
    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:NP279546.RA5vWyz6LR1BZFSPIk1bKtlcIevA7vj98Fxffp_oGPjVw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:37+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" .
}