@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP628949.RAnmvvLTBdcR6tKZmx6Olcnhn1nh0OlqfjBa-RQLawSHs> .
@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:NP628949.RAnmvvLTBdcR6tKZmx6Olcnhn1nh0OlqfjBa-RQLawSHs130_head {
  this: np:hasAssertion dgn-np:NP628949.RAnmvvLTBdcR6tKZmx6Olcnhn1nh0OlqfjBa-RQLawSHs130_assertion;
    np:hasProvenance dgn-np:NP628949.RAnmvvLTBdcR6tKZmx6Olcnhn1nh0OlqfjBa-RQLawSHs130_provenance;
    np:hasPublicationInfo dgn-np:NP628949.RAnmvvLTBdcR6tKZmx6Olcnhn1nh0OlqfjBa-RQLawSHs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP628949.RAnmvvLTBdcR6tKZmx6Olcnhn1nh0OlqfjBa-RQLawSHs130_assertion a np:Assertion .
  
  dgn-np:NP628949.RAnmvvLTBdcR6tKZmx6Olcnhn1nh0OlqfjBa-RQLawSHs130_provenance a np:Provenance .
  
  dgn-np:NP628949.RAnmvvLTBdcR6tKZmx6Olcnhn1nh0OlqfjBa-RQLawSHs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP628949.RAnmvvLTBdcR6tKZmx6Olcnhn1nh0OlqfjBa-RQLawSHs130_assertion {
  miriam-gene:2272 a ncit:C16612 .
  
  lld:C0022665 a ncit:C7057 .
  
  dgn-gda:DGNb758eae964adf5df29c1ed55b61eb048 sio:SIO_000628 miriam-gene:2272, lld:C0022665;
    a sio:SIO_001121 .
}

dgn-np:NP628949.RAnmvvLTBdcR6tKZmx6Olcnhn1nh0OlqfjBa-RQLawSHs130_provenance {
  dgn-np:NP628949.RAnmvvLTBdcR6tKZmx6Olcnhn1nh0OlqfjBa-RQLawSHs130_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:NP628949.RAnmvvLTBdcR6tKZmx6Olcnhn1nh0OlqfjBa-RQLawSHs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:19+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" .
}