@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP163597.RAv-RazyzhcICwaFtQHacKQohjpSKAlZEDCRjFUUun2bI> .
@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:NP163597.RAv-RazyzhcICwaFtQHacKQohjpSKAlZEDCRjFUUun2bI130_head {
  this: np:hasAssertion dgn-np:NP163597.RAv-RazyzhcICwaFtQHacKQohjpSKAlZEDCRjFUUun2bI130_assertion;
    np:hasProvenance dgn-np:NP163597.RAv-RazyzhcICwaFtQHacKQohjpSKAlZEDCRjFUUun2bI130_provenance;
    np:hasPublicationInfo dgn-np:NP163597.RAv-RazyzhcICwaFtQHacKQohjpSKAlZEDCRjFUUun2bI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP163597.RAv-RazyzhcICwaFtQHacKQohjpSKAlZEDCRjFUUun2bI130_assertion a np:Assertion .
  
  dgn-np:NP163597.RAv-RazyzhcICwaFtQHacKQohjpSKAlZEDCRjFUUun2bI130_provenance a np:Provenance .
  
  dgn-np:NP163597.RAv-RazyzhcICwaFtQHacKQohjpSKAlZEDCRjFUUun2bI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP163597.RAv-RazyzhcICwaFtQHacKQohjpSKAlZEDCRjFUUun2bI130_assertion {
  miriam-gene:2272 a ncit:C16612 .
  
  lld:C0152018 a ncit:C7057 .
  
  dgn-gda:DGNed83a83e1cfdec53d535db65a5c05937 sio:SIO_000628 miriam-gene:2272, lld:C0152018;
    a sio:SIO_001121 .
}

dgn-np:NP163597.RAv-RazyzhcICwaFtQHacKQohjpSKAlZEDCRjFUUun2bI130_provenance {
  dgn-np:NP163597.RAv-RazyzhcICwaFtQHacKQohjpSKAlZEDCRjFUUun2bI130_assertion dcterms:description
      "[These data suggest that the open reading frame of FHIT is not important in the development or progression of most primary esophageal carcinomas or UCANs, although lack of expression of the FHIT transcript may be common in esophageal cancer-derived cell lines.]. 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:9233782;
    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:NP163597.RAv-RazyzhcICwaFtQHacKQohjpSKAlZEDCRjFUUun2bI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:28+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" .
}