@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP742428.RAMrPF5gSrKJiRW7ziq0_iRSrnQ4oNaBcZ0hkbp_hHQvc> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP742428.RAMrPF5gSrKJiRW7ziq0_iRSrnQ4oNaBcZ0hkbp_hHQvc130_head {
  this: np:hasAssertion dgn-np:NP742428.RAMrPF5gSrKJiRW7ziq0_iRSrnQ4oNaBcZ0hkbp_hHQvc130_assertion;
    np:hasProvenance dgn-np:NP742428.RAMrPF5gSrKJiRW7ziq0_iRSrnQ4oNaBcZ0hkbp_hHQvc130_provenance;
    np:hasPublicationInfo dgn-np:NP742428.RAMrPF5gSrKJiRW7ziq0_iRSrnQ4oNaBcZ0hkbp_hHQvc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP742428.RAMrPF5gSrKJiRW7ziq0_iRSrnQ4oNaBcZ0hkbp_hHQvc130_assertion a np:Assertion .
  
  dgn-np:NP742428.RAMrPF5gSrKJiRW7ziq0_iRSrnQ4oNaBcZ0hkbp_hHQvc130_provenance a np:Provenance .
  
  dgn-np:NP742428.RAMrPF5gSrKJiRW7ziq0_iRSrnQ4oNaBcZ0hkbp_hHQvc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP742428.RAMrPF5gSrKJiRW7ziq0_iRSrnQ4oNaBcZ0hkbp_hHQvc130_assertion {
  miriam-gene:5979 a ncit:C16612 .
  
  lld:C0027627 a ncit:C7057 .
  
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    a sio:SIO_001121 .
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dgn-np:NP742428.RAMrPF5gSrKJiRW7ziq0_iRSrnQ4oNaBcZ0hkbp_hHQvc130_provenance {
  dgn-np:NP742428.RAMrPF5gSrKJiRW7ziq0_iRSrnQ4oNaBcZ0hkbp_hHQvc130_assertion dcterms:description
      "[To obtain comprehensive genetic information on advanced thyroid cancers, we designed an assay panel for mass spectrometry genotyping encompassing the most significant oncogenes in this disease: 111 mutations in RET, BRAF, NRAS, HRAS, KRAS, PIK3CA, AKT1, and other related genes were surveyed in 31 cell lines, 52 primary tumors (34 PDTC and 18 ATC), and 55 RAIR, FDG-PET-positive recurrences and metastases (nodal and distant) from 42 patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP742428.RAMrPF5gSrKJiRW7ziq0_iRSrnQ4oNaBcZ0hkbp_hHQvc130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:21+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
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    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
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    pav:version "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}