@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP786783.RAWdCKnPcpPOz0XGFRJZ0NF_rOKw-WdF7-o0FEDEdTfi8> .
@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:NP786783.RAWdCKnPcpPOz0XGFRJZ0NF_rOKw-WdF7-o0FEDEdTfi8130_head {
  this: np:hasAssertion dgn-np:NP786783.RAWdCKnPcpPOz0XGFRJZ0NF_rOKw-WdF7-o0FEDEdTfi8130_assertion;
    np:hasProvenance dgn-np:NP786783.RAWdCKnPcpPOz0XGFRJZ0NF_rOKw-WdF7-o0FEDEdTfi8130_provenance;
    np:hasPublicationInfo dgn-np:NP786783.RAWdCKnPcpPOz0XGFRJZ0NF_rOKw-WdF7-o0FEDEdTfi8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP786783.RAWdCKnPcpPOz0XGFRJZ0NF_rOKw-WdF7-o0FEDEdTfi8130_assertion a np:Assertion .
  
  dgn-np:NP786783.RAWdCKnPcpPOz0XGFRJZ0NF_rOKw-WdF7-o0FEDEdTfi8130_provenance a np:Provenance .
  
  dgn-np:NP786783.RAWdCKnPcpPOz0XGFRJZ0NF_rOKw-WdF7-o0FEDEdTfi8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP786783.RAWdCKnPcpPOz0XGFRJZ0NF_rOKw-WdF7-o0FEDEdTfi8130_assertion {
  miriam-gene:796 a ncit:C16612 .
  
  lld:C0027662 a ncit:C7057 .
  
  dgn-gda:DGNbbae76aba4e99742556d6b86674e130f sio:SIO_000628 miriam-gene:796, lld:C0027662;
    a sio:SIO_001121 .
}

dgn-np:NP786783.RAWdCKnPcpPOz0XGFRJZ0NF_rOKw-WdF7-o0FEDEdTfi8130_provenance {
  dgn-np:NP786783.RAWdCKnPcpPOz0XGFRJZ0NF_rOKw-WdF7-o0FEDEdTfi8130_assertion dcterms:description
      "[American Thyroid Association (ATA) guidelines suggest that thyroidectomy can be delayed in some children with multiple endocrine neoplasia syndrome 2A (MEN2A) if serum calcitonin (Ct) and neck ultrasonography (US) are normal.]. 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:22890595;
    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:NP786783.RAWdCKnPcpPOz0XGFRJZ0NF_rOKw-WdF7-o0FEDEdTfi8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:00+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" .
}