@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP539663.RAvD9BtSvxn5CWY3eXgY-Q2mqwfTWcGvSIo0_wNU2cDWE> .
@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:NP539663.RAvD9BtSvxn5CWY3eXgY-Q2mqwfTWcGvSIo0_wNU2cDWE130_head {
  this: np:hasAssertion dgn-np:NP539663.RAvD9BtSvxn5CWY3eXgY-Q2mqwfTWcGvSIo0_wNU2cDWE130_assertion;
    np:hasProvenance dgn-np:NP539663.RAvD9BtSvxn5CWY3eXgY-Q2mqwfTWcGvSIo0_wNU2cDWE130_provenance;
    np:hasPublicationInfo dgn-np:NP539663.RAvD9BtSvxn5CWY3eXgY-Q2mqwfTWcGvSIo0_wNU2cDWE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP539663.RAvD9BtSvxn5CWY3eXgY-Q2mqwfTWcGvSIo0_wNU2cDWE130_assertion a np:Assertion .
  
  dgn-np:NP539663.RAvD9BtSvxn5CWY3eXgY-Q2mqwfTWcGvSIo0_wNU2cDWE130_provenance a np:Provenance .
  
  dgn-np:NP539663.RAvD9BtSvxn5CWY3eXgY-Q2mqwfTWcGvSIo0_wNU2cDWE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP539663.RAvD9BtSvxn5CWY3eXgY-Q2mqwfTWcGvSIo0_wNU2cDWE130_assertion {
  miriam-gene:51741 a ncit:C16612 .
  
  lld:C0027651 a ncit:C7057 .
  
  dgn-gda:DGNf455b4d15a998234db44d9fef5daf95e sio:SIO_000628 miriam-gene:51741, lld:C0027651;
    a sio:SIO_001121 .
}

dgn-np:NP539663.RAvD9BtSvxn5CWY3eXgY-Q2mqwfTWcGvSIo0_wNU2cDWE130_provenance {
  dgn-np:NP539663.RAvD9BtSvxn5CWY3eXgY-Q2mqwfTWcGvSIo0_wNU2cDWE130_assertion dcterms:description
      "[Because the fragile histidine triad (FHIT) gene, a tumor suppressor gene encompassing the most active, common fragile site FRA3B, is frequently deleted in various cancers, we evaluated the expression of WWOX and FHIT in 74 cases of primary hematopoietic neoplasias and 20 leukemia 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:14638866;
    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:NP539663.RAvD9BtSvxn5CWY3eXgY-Q2mqwfTWcGvSIo0_wNU2cDWE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:25+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" .
}