@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP860348.RAzRNNCdgvhkq41-Tbv1ZQVookQgL5eCF-Pu97RvOi3EA> .
@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:NP860348.RAzRNNCdgvhkq41-Tbv1ZQVookQgL5eCF-Pu97RvOi3EA130_head {
  this: np:hasAssertion dgn-np:NP860348.RAzRNNCdgvhkq41-Tbv1ZQVookQgL5eCF-Pu97RvOi3EA130_assertion;
    np:hasProvenance dgn-np:NP860348.RAzRNNCdgvhkq41-Tbv1ZQVookQgL5eCF-Pu97RvOi3EA130_provenance;
    np:hasPublicationInfo dgn-np:NP860348.RAzRNNCdgvhkq41-Tbv1ZQVookQgL5eCF-Pu97RvOi3EA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP860348.RAzRNNCdgvhkq41-Tbv1ZQVookQgL5eCF-Pu97RvOi3EA130_assertion a np:Assertion .
  
  dgn-np:NP860348.RAzRNNCdgvhkq41-Tbv1ZQVookQgL5eCF-Pu97RvOi3EA130_provenance a np:Provenance .
  
  dgn-np:NP860348.RAzRNNCdgvhkq41-Tbv1ZQVookQgL5eCF-Pu97RvOi3EA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP860348.RAzRNNCdgvhkq41-Tbv1ZQVookQgL5eCF-Pu97RvOi3EA130_assertion {
  miriam-gene:5979 a ncit:C16612 .
  
  lld:C0019247 a ncit:C7057 .
  
  dgn-gda:DGN91e42d8626fc0d0f0ca4a6c55d544d84 sio:SIO_000628 miriam-gene:5979, lld:C0019247;
    a sio:SIO_001121 .
}

dgn-np:NP860348.RAzRNNCdgvhkq41-Tbv1ZQVookQgL5eCF-Pu97RvOi3EA130_provenance {
  dgn-np:NP860348.RAzRNNCdgvhkq41-Tbv1ZQVookQgL5eCF-Pu97RvOi3EA130_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-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:NP860348.RAzRNNCdgvhkq41-Tbv1ZQVookQgL5eCF-Pu97RvOi3EA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:46+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" .
}