@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP248590.RAbylKnM-sSECLBOF8Veg-Kb456A-B9febE8gSyZxl8IU> .
@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:NP248590.RAbylKnM-sSECLBOF8Veg-Kb456A-B9febE8gSyZxl8IU130_head {
  this: np:hasAssertion dgn-np:NP248590.RAbylKnM-sSECLBOF8Veg-Kb456A-B9febE8gSyZxl8IU130_assertion;
    np:hasProvenance dgn-np:NP248590.RAbylKnM-sSECLBOF8Veg-Kb456A-B9febE8gSyZxl8IU130_provenance;
    np:hasPublicationInfo dgn-np:NP248590.RAbylKnM-sSECLBOF8Veg-Kb456A-B9febE8gSyZxl8IU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP248590.RAbylKnM-sSECLBOF8Veg-Kb456A-B9febE8gSyZxl8IU130_assertion a np:Assertion .
  
  dgn-np:NP248590.RAbylKnM-sSECLBOF8Veg-Kb456A-B9febE8gSyZxl8IU130_provenance a np:Provenance .
  
  dgn-np:NP248590.RAbylKnM-sSECLBOF8Veg-Kb456A-B9febE8gSyZxl8IU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP248590.RAbylKnM-sSECLBOF8Veg-Kb456A-B9febE8gSyZxl8IU130_assertion {
  miriam-gene:3081 a ncit:C16612 .
  
  lld:C0279628 a ncit:C7057 .
  
  dgn-gda:DGN93f7c14d61a8c80acecd7a0cc81d3bbc sio:SIO_000628 miriam-gene:3081, lld:C0279628;
    a sio:SIO_001121 .
}

dgn-np:NP248590.RAbylKnM-sSECLBOF8Veg-Kb456A-B9febE8gSyZxl8IU130_provenance {
  dgn-np:NP248590.RAbylKnM-sSECLBOF8Veg-Kb456A-B9febE8gSyZxl8IU130_assertion dcterms:description
      "[These findings suggest that FISH has high sensitivity for the detection of dysplasia and EA in BE patients, with the power to stratify patients by FISH abnormality for progression to HGD/EA.]. 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:18602665;
    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:NP248590.RAbylKnM-sSECLBOF8Veg-Kb456A-B9febE8gSyZxl8IU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:19+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" .
}