@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP933581.RAyFcEmUlosnDPvkftxZ1JZlwA7vOG_M9a6hhg0jB_m90> .
@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:NP933581.RAyFcEmUlosnDPvkftxZ1JZlwA7vOG_M9a6hhg0jB_m90130_head {
  this: np:hasAssertion dgn-np:NP933581.RAyFcEmUlosnDPvkftxZ1JZlwA7vOG_M9a6hhg0jB_m90130_assertion;
    np:hasProvenance dgn-np:NP933581.RAyFcEmUlosnDPvkftxZ1JZlwA7vOG_M9a6hhg0jB_m90130_provenance;
    np:hasPublicationInfo dgn-np:NP933581.RAyFcEmUlosnDPvkftxZ1JZlwA7vOG_M9a6hhg0jB_m90130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP933581.RAyFcEmUlosnDPvkftxZ1JZlwA7vOG_M9a6hhg0jB_m90130_assertion a np:Assertion .
  
  dgn-np:NP933581.RAyFcEmUlosnDPvkftxZ1JZlwA7vOG_M9a6hhg0jB_m90130_provenance a np:Provenance .
  
  dgn-np:NP933581.RAyFcEmUlosnDPvkftxZ1JZlwA7vOG_M9a6hhg0jB_m90130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP933581.RAyFcEmUlosnDPvkftxZ1JZlwA7vOG_M9a6hhg0jB_m90130_assertion {
  miriam-gene:2272 a ncit:C16612 .
  
  lld:C0279702 a ncit:C7057 .
  
  dgn-gda:DGN9d3cadb5b39056ec248171a276b2dabc sio:SIO_000628 miriam-gene:2272, lld:C0279702;
    a sio:SIO_001121 .
}

dgn-np:NP933581.RAyFcEmUlosnDPvkftxZ1JZlwA7vOG_M9a6hhg0jB_m90130_provenance {
  dgn-np:NP933581.RAyFcEmUlosnDPvkftxZ1JZlwA7vOG_M9a6hhg0jB_m90130_assertion dcterms:description
      "[Since genetic alterations were not frequently observed in DNA corresponding to the FHIT gene in renal tumours, to elucidate the mechanism of FHIT gene silencing we examined 22 paired samples of clear cell renal carcinoma and non-malignant renal tissue for the methylation of the FHIT 5'CpG island by methylation-specific PCR.]. 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:18378390;
    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:NP933581.RAyFcEmUlosnDPvkftxZ1JZlwA7vOG_M9a6hhg0jB_m90130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:32+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" .
}