@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP532781.RAMzc3FnSr9w4V2Tdr5iVb6cd1JS958FLIKcgOLszkLOw> .
@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:NP532781.RAMzc3FnSr9w4V2Tdr5iVb6cd1JS958FLIKcgOLszkLOw130_head {
  this: np:hasAssertion dgn-np:NP532781.RAMzc3FnSr9w4V2Tdr5iVb6cd1JS958FLIKcgOLszkLOw130_assertion;
    np:hasProvenance dgn-np:NP532781.RAMzc3FnSr9w4V2Tdr5iVb6cd1JS958FLIKcgOLszkLOw130_provenance;
    np:hasPublicationInfo dgn-np:NP532781.RAMzc3FnSr9w4V2Tdr5iVb6cd1JS958FLIKcgOLszkLOw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP532781.RAMzc3FnSr9w4V2Tdr5iVb6cd1JS958FLIKcgOLszkLOw130_assertion a np:Assertion .
  
  dgn-np:NP532781.RAMzc3FnSr9w4V2Tdr5iVb6cd1JS958FLIKcgOLszkLOw130_provenance a np:Provenance .
  
  dgn-np:NP532781.RAMzc3FnSr9w4V2Tdr5iVb6cd1JS958FLIKcgOLszkLOw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP532781.RAMzc3FnSr9w4V2Tdr5iVb6cd1JS958FLIKcgOLszkLOw130_assertion {
  miriam-gene:472 a ncit:C16612 .
  
  lld:C0206682 a ncit:C7057 .
  
  dgn-gda:DGN450a8f83e6305b1820445a8b4066bd4a sio:SIO_000628 miriam-gene:472, lld:C0206682;
    a sio:SIO_001121 .
}

dgn-np:NP532781.RAMzc3FnSr9w4V2Tdr5iVb6cd1JS958FLIKcgOLszkLOw130_provenance {
  dgn-np:NP532781.RAMzc3FnSr9w4V2Tdr5iVb6cd1JS958FLIKcgOLszkLOw130_assertion dcterms:description
      "[These results unveil the chromosomal regions where genes of interest in thyroid anaplastic transformation are to be located, and demonstrate that different gene dosage copy sequence imbalances are associated to the 'direct' pathway of transformation of follicular into anaplastic cancers and to the progressive FTC --> PDTC --> ATC pathway.]. 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:14735198;
    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:NP532781.RAMzc3FnSr9w4V2Tdr5iVb6cd1JS958FLIKcgOLszkLOw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:21+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" .
}