@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1408926.RAVyNQSIjhP553hiOe1wtREUaHHFnYl_IzqBVZ02UlsZA> .
@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:NP1408926.RAVyNQSIjhP553hiOe1wtREUaHHFnYl_IzqBVZ02UlsZA130_head {
  this: np:hasAssertion dgn-np:NP1408926.RAVyNQSIjhP553hiOe1wtREUaHHFnYl_IzqBVZ02UlsZA130_assertion;
    np:hasProvenance dgn-np:NP1408926.RAVyNQSIjhP553hiOe1wtREUaHHFnYl_IzqBVZ02UlsZA130_provenance;
    np:hasPublicationInfo dgn-np:NP1408926.RAVyNQSIjhP553hiOe1wtREUaHHFnYl_IzqBVZ02UlsZA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1408926.RAVyNQSIjhP553hiOe1wtREUaHHFnYl_IzqBVZ02UlsZA130_assertion a np:Assertion .
  
  dgn-np:NP1408926.RAVyNQSIjhP553hiOe1wtREUaHHFnYl_IzqBVZ02UlsZA130_provenance a np:Provenance .
  
  dgn-np:NP1408926.RAVyNQSIjhP553hiOe1wtREUaHHFnYl_IzqBVZ02UlsZA130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1408926.RAVyNQSIjhP553hiOe1wtREUaHHFnYl_IzqBVZ02UlsZA130_assertion {
  miriam-gene:5979 a ncit:C16612 .
  
  lld:C0027662 a ncit:C7057 .
  
  dgn-gda:DGNf3fb1aefe312be4a1d2f93e88befc2bf sio:SIO_000628 miriam-gene:5979, lld:C0027662;
    a sio:SIO_001121 .
}

dgn-np:NP1408926.RAVyNQSIjhP553hiOe1wtREUaHHFnYl_IzqBVZ02UlsZA130_provenance {
  dgn-np:NP1408926.RAVyNQSIjhP553hiOe1wtREUaHHFnYl_IzqBVZ02UlsZA130_assertion dcterms:description
      "[Despite advances in the understanding of the genotype-phenotype correlation in multiple endocrine neoplasia type 2A and 2B (multiple endocrine neoplasia (MEN) 2A, MEN 2B), and familial medullary thyroid carcinoma (FMTC), the frequency and prognostic relevance of RET protooncogene mutations in sporadic medullary thyroid carcinomas (MTCs) remain controversial.]. 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:9818022;
    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:NP1408926.RAVyNQSIjhP553hiOe1wtREUaHHFnYl_IzqBVZ02UlsZA130_publicationInfo {
  this: dcterms:created "2016-05-13T12:52:25+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}