@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP163370.RAVMg4sY94diFzZ3frOEYQrAt3nBnfzvN9ZOA2SVzXkSc> .
@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:NP163370.RAVMg4sY94diFzZ3frOEYQrAt3nBnfzvN9ZOA2SVzXkSc130_head {
  this: np:hasAssertion dgn-np:NP163370.RAVMg4sY94diFzZ3frOEYQrAt3nBnfzvN9ZOA2SVzXkSc130_assertion;
    np:hasProvenance dgn-np:NP163370.RAVMg4sY94diFzZ3frOEYQrAt3nBnfzvN9ZOA2SVzXkSc130_provenance;
    np:hasPublicationInfo dgn-np:NP163370.RAVMg4sY94diFzZ3frOEYQrAt3nBnfzvN9ZOA2SVzXkSc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP163370.RAVMg4sY94diFzZ3frOEYQrAt3nBnfzvN9ZOA2SVzXkSc130_assertion a np:Assertion .
  
  dgn-np:NP163370.RAVMg4sY94diFzZ3frOEYQrAt3nBnfzvN9ZOA2SVzXkSc130_provenance a np:Provenance .
  
  dgn-np:NP163370.RAVMg4sY94diFzZ3frOEYQrAt3nBnfzvN9ZOA2SVzXkSc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP163370.RAVMg4sY94diFzZ3frOEYQrAt3nBnfzvN9ZOA2SVzXkSc130_assertion {
  miriam-gene:7248 a ncit:C16612 .
  
  lld:C0040136 a ncit:C7057 .
  
  dgn-gda:DGN5c3e77beea4ce343b8b7d753dd80b622 sio:SIO_000628 miriam-gene:7248, lld:C0040136;
    a sio:SIO_001121 .
}

dgn-np:NP163370.RAVMg4sY94diFzZ3frOEYQrAt3nBnfzvN9ZOA2SVzXkSc130_provenance {
  dgn-np:NP163370.RAVMg4sY94diFzZ3frOEYQrAt3nBnfzvN9ZOA2SVzXkSc130_assertion dcterms:description
      "[Given that defective FHIT genes were found in both benign and malignant thyroid tumours, the inactivation of this putative tumour suppressor gene is likely to be an early event in the pathogenesis of some forms of thyroid neoplasms.]. 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:10448301;
    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:NP163370.RAVMg4sY94diFzZ3frOEYQrAt3nBnfzvN9ZOA2SVzXkSc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:28+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" .
}