@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP782060.RAyBfDHnTa6iszvZKENuMC-O5DllzSxOU8CPJyGru6iug> .
@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:NP782060.RAyBfDHnTa6iszvZKENuMC-O5DllzSxOU8CPJyGru6iug130_head {
  this: np:hasAssertion dgn-np:NP782060.RAyBfDHnTa6iszvZKENuMC-O5DllzSxOU8CPJyGru6iug130_assertion ;
    np:hasProvenance dgn-np:NP782060.RAyBfDHnTa6iszvZKENuMC-O5DllzSxOU8CPJyGru6iug130_provenance ;
    np:hasPublicationInfo dgn-np:NP782060.RAyBfDHnTa6iszvZKENuMC-O5DllzSxOU8CPJyGru6iug130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP782060.RAyBfDHnTa6iszvZKENuMC-O5DllzSxOU8CPJyGru6iug130_assertion a np:Assertion .
  dgn-np:NP782060.RAyBfDHnTa6iszvZKENuMC-O5DllzSxOU8CPJyGru6iug130_provenance a np:Provenance .
  dgn-np:NP782060.RAyBfDHnTa6iszvZKENuMC-O5DllzSxOU8CPJyGru6iug130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP782060.RAyBfDHnTa6iszvZKENuMC-O5DllzSxOU8CPJyGru6iug130_assertion {
  miriam-gene:2272 a ncit:C16612 .
  lld:C0940937 a ncit:C7057 .
  dgn-gda:DGNacf0a3d92a21a1b28814542d90129db7 sio:SIO_000628 miriam-gene:2272 , lld:C0940937 ;
    a sio:SIO_001121 .
}
dgn-np:NP782060.RAyBfDHnTa6iszvZKENuMC-O5DllzSxOU8CPJyGru6iug130_provenance {
  dgn-np:NP782060.RAyBfDHnTa6iszvZKENuMC-O5DllzSxOU8CPJyGru6iug130_assertion dcterms:description "[More than 12 years and >800 scientific publications after the discovery of the first gene at a chromosome fragile site, the FHIT gene at FRA3B, there are still questions to pursue concerning the selective advantage conferred to cells by loss of expression of FHIT, the most frequent target of allele deletion in precancerous lesions and cancers.]. 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:20082323 ;
    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:NP782060.RAyBfDHnTa6iszvZKENuMC-O5DllzSxOU8CPJyGru6iug130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:54+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" .
}