@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP497529.RAd7M5ul5nLwG6-17Um_9s8hd-y2TNEZcUINsOU6HxYJk> .
@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:NP497529.RAd7M5ul5nLwG6-17Um_9s8hd-y2TNEZcUINsOU6HxYJk130_head {
  this: np:hasAssertion dgn-np:NP497529.RAd7M5ul5nLwG6-17Um_9s8hd-y2TNEZcUINsOU6HxYJk130_assertion ;
    np:hasProvenance dgn-np:NP497529.RAd7M5ul5nLwG6-17Um_9s8hd-y2TNEZcUINsOU6HxYJk130_provenance ;
    np:hasPublicationInfo dgn-np:NP497529.RAd7M5ul5nLwG6-17Um_9s8hd-y2TNEZcUINsOU6HxYJk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP497529.RAd7M5ul5nLwG6-17Um_9s8hd-y2TNEZcUINsOU6HxYJk130_assertion a np:Assertion .
  dgn-np:NP497529.RAd7M5ul5nLwG6-17Um_9s8hd-y2TNEZcUINsOU6HxYJk130_provenance a np:Provenance .
  dgn-np:NP497529.RAd7M5ul5nLwG6-17Um_9s8hd-y2TNEZcUINsOU6HxYJk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP497529.RAd7M5ul5nLwG6-17Um_9s8hd-y2TNEZcUINsOU6HxYJk130_assertion {
  miriam-gene:2272 a ncit:C16612 .
  lld:C0178874 a ncit:C7057 .
  dgn-gda:DGNa1017e8df4022f4d99bee6ee96892c7f sio:SIO_000628 miriam-gene:2272 , lld:C0178874 ;
    a sio:SIO_001121 .
}
dgn-np:NP497529.RAd7M5ul5nLwG6-17Um_9s8hd-y2TNEZcUINsOU6HxYJk130_provenance {
  dgn-np:NP497529.RAd7M5ul5nLwG6-17Um_9s8hd-y2TNEZcUINsOU6HxYJk130_assertion dcterms:description "[Simultaneous scanning of FHIT and WWOX exons in the context of early tumorigenesis and tumor progression, may help clarify the mechanistic events related to cancer development which are not revealed by immuno histochemistry assays.]. 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:16895604 ;
    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:NP497529.RAd7M5ul5nLwG6-17Um_9s8hd-y2TNEZcUINsOU6HxYJk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:57+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" .
}