@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1173636.RADlzktbgcuhxkmIBt2Ol5vZBEaBKmDUGeJgEMmvHNqBk> .
@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/v4.0.0/void/> .

dgn-np:NP1173636.RADlzktbgcuhxkmIBt2Ol5vZBEaBKmDUGeJgEMmvHNqBk130_head {
  this: np:hasAssertion dgn-np:NP1173636.RADlzktbgcuhxkmIBt2Ol5vZBEaBKmDUGeJgEMmvHNqBk130_assertion;
    np:hasProvenance dgn-np:NP1173636.RADlzktbgcuhxkmIBt2Ol5vZBEaBKmDUGeJgEMmvHNqBk130_provenance;
    np:hasPublicationInfo dgn-np:NP1173636.RADlzktbgcuhxkmIBt2Ol5vZBEaBKmDUGeJgEMmvHNqBk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1173636.RADlzktbgcuhxkmIBt2Ol5vZBEaBKmDUGeJgEMmvHNqBk130_assertion a np:Assertion .
  
  dgn-np:NP1173636.RADlzktbgcuhxkmIBt2Ol5vZBEaBKmDUGeJgEMmvHNqBk130_provenance a np:Provenance .
  
  dgn-np:NP1173636.RADlzktbgcuhxkmIBt2Ol5vZBEaBKmDUGeJgEMmvHNqBk130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1173636.RADlzktbgcuhxkmIBt2Ol5vZBEaBKmDUGeJgEMmvHNqBk130_assertion {
  miriam-gene:7173 a ncit:C16612 .
  
  lld:C0018021 a ncit:C7057 .
  
  dgn-gda:DGNd112e8b20d4becb594845c3725182e2c sio:SIO_000628 miriam-gene:7173, lld:C0018021;
    a sio:SIO_001121 .
}

dgn-np:NP1173636.RADlzktbgcuhxkmIBt2Ol5vZBEaBKmDUGeJgEMmvHNqBk130_provenance {
  dgn-np:NP1173636.RADlzktbgcuhxkmIBt2Ol5vZBEaBKmDUGeJgEMmvHNqBk130_assertion dcterms:description
      "[The aim of this study was to screen for DUOX2, TPO and TG mutations in Chinese patients with congenital hypothyroidism (CH) and goitre and to define the relationships between DUOX2 genotypes and clinical phenotypes.]. 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:24735383;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1173636.RADlzktbgcuhxkmIBt2Ol5vZBEaBKmDUGeJgEMmvHNqBk130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:38+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}