@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP662355.RAhEWVC4EHix1T1_0TkfCEQ19SPKSC28eTjjvqoY4y8Wc> .
@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:NP662355.RAhEWVC4EHix1T1_0TkfCEQ19SPKSC28eTjjvqoY4y8Wc130_head {
  this: np:hasAssertion dgn-np:NP662355.RAhEWVC4EHix1T1_0TkfCEQ19SPKSC28eTjjvqoY4y8Wc130_assertion;
    np:hasProvenance dgn-np:NP662355.RAhEWVC4EHix1T1_0TkfCEQ19SPKSC28eTjjvqoY4y8Wc130_provenance;
    np:hasPublicationInfo dgn-np:NP662355.RAhEWVC4EHix1T1_0TkfCEQ19SPKSC28eTjjvqoY4y8Wc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP662355.RAhEWVC4EHix1T1_0TkfCEQ19SPKSC28eTjjvqoY4y8Wc130_assertion a np:Assertion .
  
  dgn-np:NP662355.RAhEWVC4EHix1T1_0TkfCEQ19SPKSC28eTjjvqoY4y8Wc130_provenance a np:Provenance .
  
  dgn-np:NP662355.RAhEWVC4EHix1T1_0TkfCEQ19SPKSC28eTjjvqoY4y8Wc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP662355.RAhEWVC4EHix1T1_0TkfCEQ19SPKSC28eTjjvqoY4y8Wc130_assertion {
  miriam-gene:7038 a ncit:C16612 .
  
  lld:C0020550 a ncit:C7057 .
  
  dgn-gda:DGN8badd739d901542bf2e85856366a19f8 sio:SIO_000628 miriam-gene:7038, lld:C0020550;
    a sio:SIO_001121 .
}

dgn-np:NP662355.RAhEWVC4EHix1T1_0TkfCEQ19SPKSC28eTjjvqoY4y8Wc130_provenance {
  dgn-np:NP662355.RAhEWVC4EHix1T1_0TkfCEQ19SPKSC28eTjjvqoY4y8Wc130_assertion dcterms:description
      "[Because of the diffuse (99 m)Tc uptake and the negative TPO, TSHR, and thyroglobulin antibodies, genetic analysis of her TSHR gene was performed, in spite of her negative family history for hyperthyroidism.]. 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:22763653;
    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:NP662355.RAhEWVC4EHix1T1_0TkfCEQ19SPKSC28eTjjvqoY4y8Wc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:40+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" .
}