@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP494135.RAyexXz_WmIFonyPket77DhUu1sbQJEzj7Tj4fB3Gy498> .
@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:NP494135.RAyexXz_WmIFonyPket77DhUu1sbQJEzj7Tj4fB3Gy498130_head {
  this: np:hasAssertion dgn-np:NP494135.RAyexXz_WmIFonyPket77DhUu1sbQJEzj7Tj4fB3Gy498130_assertion;
    np:hasProvenance dgn-np:NP494135.RAyexXz_WmIFonyPket77DhUu1sbQJEzj7Tj4fB3Gy498130_provenance;
    np:hasPublicationInfo dgn-np:NP494135.RAyexXz_WmIFonyPket77DhUu1sbQJEzj7Tj4fB3Gy498130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP494135.RAyexXz_WmIFonyPket77DhUu1sbQJEzj7Tj4fB3Gy498130_assertion a np:Assertion .
  
  dgn-np:NP494135.RAyexXz_WmIFonyPket77DhUu1sbQJEzj7Tj4fB3Gy498130_provenance a np:Provenance .
  
  dgn-np:NP494135.RAyexXz_WmIFonyPket77DhUu1sbQJEzj7Tj4fB3Gy498130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP494135.RAyexXz_WmIFonyPket77DhUu1sbQJEzj7Tj4fB3Gy498130_assertion {
  miriam-gene:2272 a ncit:C16612 .
  
  lld:C1168401 a ncit:C7057 .
  
  dgn-gda:DGNbf8eedbdeaccf4f8a6a7615da0025139 sio:SIO_000628 miriam-gene:2272, lld:C1168401;
    a sio:SIO_001121 .
}

dgn-np:NP494135.RAyexXz_WmIFonyPket77DhUu1sbQJEzj7Tj4fB3Gy498130_provenance {
  dgn-np:NP494135.RAyexXz_WmIFonyPket77DhUu1sbQJEzj7Tj4fB3Gy498130_assertion dcterms:description
      "[To determine whether the FHIT gene at 3p14.2 is altered in head and neck squamous cell carcinomas (HNSCC), we examined 26 HNSCC cell lines for deletions within the FHIT locus by Southern analysis, for allelic losses of specific exons FHIT by fluorescence in situ hybridization (FISH) and for integrity of FHIT transcripts.]. 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:8790406;
    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:NP494135.RAyexXz_WmIFonyPket77DhUu1sbQJEzj7Tj4fB3Gy498130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:55+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" .
}