@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP571892.RA7MbRExELksKMl6wDClf4OTmi6XpTaXu3I-vNKVLY74c> .
@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/v3.0.0/void/> .

dgn-np:NP571892.RA7MbRExELksKMl6wDClf4OTmi6XpTaXu3I-vNKVLY74c130_head {
  this: np:hasAssertion dgn-np:NP571892.RA7MbRExELksKMl6wDClf4OTmi6XpTaXu3I-vNKVLY74c130_assertion;
    np:hasProvenance dgn-np:NP571892.RA7MbRExELksKMl6wDClf4OTmi6XpTaXu3I-vNKVLY74c130_provenance;
    np:hasPublicationInfo dgn-np:NP571892.RA7MbRExELksKMl6wDClf4OTmi6XpTaXu3I-vNKVLY74c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP571892.RA7MbRExELksKMl6wDClf4OTmi6XpTaXu3I-vNKVLY74c130_assertion a np:Assertion .
  
  dgn-np:NP571892.RA7MbRExELksKMl6wDClf4OTmi6XpTaXu3I-vNKVLY74c130_provenance a np:Provenance .
  
  dgn-np:NP571892.RA7MbRExELksKMl6wDClf4OTmi6XpTaXu3I-vNKVLY74c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP571892.RA7MbRExELksKMl6wDClf4OTmi6XpTaXu3I-vNKVLY74c130_assertion {
  miriam-gene:4489 a ncit:C16612 .
  
  lld:C0025268 a ncit:C7057 .
  
  dgn-gda:DGNe320ed03efecc11f7e726cfc1c49e7b2 sio:SIO_000628 miriam-gene:4489, lld:C0025268;
    a sio:SIO_001121 .
}

dgn-np:NP571892.RA7MbRExELksKMl6wDClf4OTmi6XpTaXu3I-vNKVLY74c130_provenance {
  dgn-np:NP571892.RA7MbRExELksKMl6wDClf4OTmi6XpTaXu3I-vNKVLY74c130_assertion dcterms:description
      "[Multiple endocrine neoplasia 2a (MEN2a) syndrome is one of the rare genetic disorder where prophylactic thyroidectomy is recommended for RET mutation carriers due to increased risk for developing MTC during lifetime.]. 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:22715565;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP571892.RA7MbRExELksKMl6wDClf4OTmi6XpTaXu3I-vNKVLY74c130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:20+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}