@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP297251.RAhMChWcG2ScaSnxZyFLaUStEgzU_Qxpu1r4eIgWTHQ8c> .
@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:NP297251.RAhMChWcG2ScaSnxZyFLaUStEgzU_Qxpu1r4eIgWTHQ8c130_head {
  this: np:hasAssertion dgn-np:NP297251.RAhMChWcG2ScaSnxZyFLaUStEgzU_Qxpu1r4eIgWTHQ8c130_assertion;
    np:hasProvenance dgn-np:NP297251.RAhMChWcG2ScaSnxZyFLaUStEgzU_Qxpu1r4eIgWTHQ8c130_provenance;
    np:hasPublicationInfo dgn-np:NP297251.RAhMChWcG2ScaSnxZyFLaUStEgzU_Qxpu1r4eIgWTHQ8c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP297251.RAhMChWcG2ScaSnxZyFLaUStEgzU_Qxpu1r4eIgWTHQ8c130_assertion a np:Assertion .
  
  dgn-np:NP297251.RAhMChWcG2ScaSnxZyFLaUStEgzU_Qxpu1r4eIgWTHQ8c130_provenance a np:Provenance .
  
  dgn-np:NP297251.RAhMChWcG2ScaSnxZyFLaUStEgzU_Qxpu1r4eIgWTHQ8c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP297251.RAhMChWcG2ScaSnxZyFLaUStEgzU_Qxpu1r4eIgWTHQ8c130_assertion {
  miriam-gene:140805 a ncit:C16612 .
  
  lld:C0040128 a ncit:C7057 .
  
  dgn-gda:DGNc94a6c51be78e7b035abb0e43c1fb1cc sio:SIO_000628 miriam-gene:140805, lld:C0040128;
    a sio:SIO_001121 .
}

dgn-np:NP297251.RAhMChWcG2ScaSnxZyFLaUStEgzU_Qxpu1r4eIgWTHQ8c130_provenance {
  dgn-np:NP297251.RAhMChWcG2ScaSnxZyFLaUStEgzU_Qxpu1r4eIgWTHQ8c130_assertion dcterms:description
      "[The purpose of the present study was to investigate the frequency of BRAF mutations in human papillary thyroid carcinoma (PTC) and Hashimoto's thyroiditis (HT) and to evaluate the association of the BRAF mutation with the clinicopathological features of both of these thyroid disorders.]. 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:16143028;
    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:NP297251.RAhMChWcG2ScaSnxZyFLaUStEgzU_Qxpu1r4eIgWTHQ8c130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:49+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" .
}