@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP161367.RAi9gjtJb2zV73rcIVytqhz6T0coM1tO1tkBTOs8EzChc> .
@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:NP161367.RAi9gjtJb2zV73rcIVytqhz6T0coM1tO1tkBTOs8EzChc130_head {
  this: np:hasAssertion dgn-np:NP161367.RAi9gjtJb2zV73rcIVytqhz6T0coM1tO1tkBTOs8EzChc130_assertion;
    np:hasProvenance dgn-np:NP161367.RAi9gjtJb2zV73rcIVytqhz6T0coM1tO1tkBTOs8EzChc130_provenance;
    np:hasPublicationInfo dgn-np:NP161367.RAi9gjtJb2zV73rcIVytqhz6T0coM1tO1tkBTOs8EzChc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP161367.RAi9gjtJb2zV73rcIVytqhz6T0coM1tO1tkBTOs8EzChc130_assertion a np:Assertion .
  
  dgn-np:NP161367.RAi9gjtJb2zV73rcIVytqhz6T0coM1tO1tkBTOs8EzChc130_provenance a np:Provenance .
  
  dgn-np:NP161367.RAi9gjtJb2zV73rcIVytqhz6T0coM1tO1tkBTOs8EzChc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP161367.RAi9gjtJb2zV73rcIVytqhz6T0coM1tO1tkBTOs8EzChc130_assertion {
  miriam-gene:4914 a ncit:C16612 .
  
  lld:C0025268 a ncit:C7057 .
  
  dgn-gda:DGN003190af5617119ce35f9b1976356084 sio:SIO_000628 miriam-gene:4914, lld:C0025268;
    a sio:SIO_001121 .
}

dgn-np:NP161367.RAi9gjtJb2zV73rcIVytqhz6T0coM1tO1tkBTOs8EzChc130_provenance {
  dgn-np:NP161367.RAi9gjtJb2zV73rcIVytqhz6T0coM1tO1tkBTOs8EzChc130_assertion dcterms:description
      "[Although no transcripts were detected in the normal portion of the thyroid from one MEN 2A patient, faint signals were detected in normal adrenal glands by Northern blot analysis, probably due to minor populations of C-cells and chromaffin cells in specimens from which MTC and pheochromocytoma might later develop.]. 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:1362408;
    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:NP161367.RAi9gjtJb2zV73rcIVytqhz6T0coM1tO1tkBTOs8EzChc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:27+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" .
}