@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP180679.RAbDsK15ZPBrfh9csLLGnYKD-iSOhHWJm2zmnE2U5cqgc> .
@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:NP180679.RAbDsK15ZPBrfh9csLLGnYKD-iSOhHWJm2zmnE2U5cqgc130_head {
  this: np:hasAssertion dgn-np:NP180679.RAbDsK15ZPBrfh9csLLGnYKD-iSOhHWJm2zmnE2U5cqgc130_assertion;
    np:hasProvenance dgn-np:NP180679.RAbDsK15ZPBrfh9csLLGnYKD-iSOhHWJm2zmnE2U5cqgc130_provenance;
    np:hasPublicationInfo dgn-np:NP180679.RAbDsK15ZPBrfh9csLLGnYKD-iSOhHWJm2zmnE2U5cqgc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP180679.RAbDsK15ZPBrfh9csLLGnYKD-iSOhHWJm2zmnE2U5cqgc130_assertion a np:Assertion .
  
  dgn-np:NP180679.RAbDsK15ZPBrfh9csLLGnYKD-iSOhHWJm2zmnE2U5cqgc130_provenance a np:Provenance .
  
  dgn-np:NP180679.RAbDsK15ZPBrfh9csLLGnYKD-iSOhHWJm2zmnE2U5cqgc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP180679.RAbDsK15ZPBrfh9csLLGnYKD-iSOhHWJm2zmnE2U5cqgc130_assertion {
  miriam-gene:5979 a ncit:C16612 .
  
  lld:C0262587 a ncit:C7057 .
  
  dgn-gda:DGNfc0fe695c93220b04fdf0336f05d4f77 sio:SIO_000628 miriam-gene:5979, lld:C0262587;
    a sio:SIO_001121 .
}

dgn-np:NP180679.RAbDsK15ZPBrfh9csLLGnYKD-iSOhHWJm2zmnE2U5cqgc130_provenance {
  dgn-np:NP180679.RAbDsK15ZPBrfh9csLLGnYKD-iSOhHWJm2zmnE2U5cqgc130_assertion dcterms:description
      "[Direct sequencing for RET exon 10, 11, 12, 13, 14, 15 and 16 and immunohistochemistry for RET monoclonal antibody were performed on the archival tissues of 84 cases of sporadic endocrine tumours, including 22 medullary thyroid carcinomas (MTCs), 35 adrenal pheochromocytomas (APCs), 18 paragangliomas (PGs), and nine parathyroid adenomas (PTAs).]. 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:15875728;
    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:NP180679.RAbDsK15ZPBrfh9csLLGnYKD-iSOhHWJm2zmnE2U5cqgc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:38+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" .
}