@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP756921.RANrGmTdZhWKqFUtBUIjLaGyc2DO_oE3VxJcu5Tlg-OR0> .
@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:NP756921.RANrGmTdZhWKqFUtBUIjLaGyc2DO_oE3VxJcu5Tlg-OR0130_head {
  this: np:hasAssertion dgn-np:NP756921.RANrGmTdZhWKqFUtBUIjLaGyc2DO_oE3VxJcu5Tlg-OR0130_assertion;
    np:hasProvenance dgn-np:NP756921.RANrGmTdZhWKqFUtBUIjLaGyc2DO_oE3VxJcu5Tlg-OR0130_provenance;
    np:hasPublicationInfo dgn-np:NP756921.RANrGmTdZhWKqFUtBUIjLaGyc2DO_oE3VxJcu5Tlg-OR0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP756921.RANrGmTdZhWKqFUtBUIjLaGyc2DO_oE3VxJcu5Tlg-OR0130_assertion a np:Assertion .
  
  dgn-np:NP756921.RANrGmTdZhWKqFUtBUIjLaGyc2DO_oE3VxJcu5Tlg-OR0130_provenance a np:Provenance .
  
  dgn-np:NP756921.RANrGmTdZhWKqFUtBUIjLaGyc2DO_oE3VxJcu5Tlg-OR0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP756921.RANrGmTdZhWKqFUtBUIjLaGyc2DO_oE3VxJcu5Tlg-OR0130_assertion {
  miriam-gene:7173 a ncit:C16612 .
  
  lld:C0549473 a ncit:C7057 .
  
  dgn-gda:DGNf2622b77e6f00dbcb431d8b62f7fd748 sio:SIO_000628 miriam-gene:7173, lld:C0549473;
    a sio:SIO_001121 .
}

dgn-np:NP756921.RANrGmTdZhWKqFUtBUIjLaGyc2DO_oE3VxJcu5Tlg-OR0130_provenance {
  dgn-np:NP756921.RANrGmTdZhWKqFUtBUIjLaGyc2DO_oE3VxJcu5Tlg-OR0130_assertion dcterms:description
      "[The occurrence of thyroid carcinoma in patients with congenital hypothyroidism (CH) caused by dyshormonogenesis is very rare, and has only been reported in one patient harboring mutations in the thyroid peroxidase (TPO) gene.]. 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:22435912;
    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:NP756921.RANrGmTdZhWKqFUtBUIjLaGyc2DO_oE3VxJcu5Tlg-OR0130_publicationInfo {
  this: dcterms:created "2015-08-25T14:45:17+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" .
}