@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP389883.RACQtuTVvkOznZTPhPTR6KqDpdQCR7ZClttpTun8Z9bEE> .
@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:NP389883.RACQtuTVvkOznZTPhPTR6KqDpdQCR7ZClttpTun8Z9bEE130_head {
  this: np:hasAssertion dgn-np:NP389883.RACQtuTVvkOznZTPhPTR6KqDpdQCR7ZClttpTun8Z9bEE130_assertion;
    np:hasProvenance dgn-np:NP389883.RACQtuTVvkOznZTPhPTR6KqDpdQCR7ZClttpTun8Z9bEE130_provenance;
    np:hasPublicationInfo dgn-np:NP389883.RACQtuTVvkOznZTPhPTR6KqDpdQCR7ZClttpTun8Z9bEE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP389883.RACQtuTVvkOznZTPhPTR6KqDpdQCR7ZClttpTun8Z9bEE130_assertion a np:Assertion .
  
  dgn-np:NP389883.RACQtuTVvkOznZTPhPTR6KqDpdQCR7ZClttpTun8Z9bEE130_provenance a np:Provenance .
  
  dgn-np:NP389883.RACQtuTVvkOznZTPhPTR6KqDpdQCR7ZClttpTun8Z9bEE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP389883.RACQtuTVvkOznZTPhPTR6KqDpdQCR7ZClttpTun8Z9bEE130_assertion {
  miriam-gene:2070 a ncit:C16612 .
  
  lld:C0546837 a ncit:C7057 .
  
  dgn-gda:DGN3c4229adccfe4b8e3633110045a7ee43 sio:SIO_000628 miriam-gene:2070, lld:C0546837;
    a sio:SIO_001121 .
}

dgn-np:NP389883.RACQtuTVvkOznZTPhPTR6KqDpdQCR7ZClttpTun8Z9bEE130_provenance {
  dgn-np:NP389883.RACQtuTVvkOznZTPhPTR6KqDpdQCR7ZClttpTun8Z9bEE130_assertion dcterms:description
      "[The testing sensitivities in the predicting ESCD and ESCC in the discriminant model including EYA4 and hTERT and the five traditional risk factors (sex, age, smoking, alcohol drinking, and family history of esophageal cancer) were 70% and 80%, and testing specificities were 76% and 88% respectively.]. 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:19939248;
    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:NP389883.RACQtuTVvkOznZTPhPTR6KqDpdQCR7ZClttpTun8Z9bEE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:52+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" .
}