@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1173637.RApInDgMw956C_92IeBXQlb0ls12-e0Gr2657XVFagf6w> .
@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:NP1173637.RApInDgMw956C_92IeBXQlb0ls12-e0Gr2657XVFagf6w130_head {
  this: np:hasAssertion dgn-np:NP1173637.RApInDgMw956C_92IeBXQlb0ls12-e0Gr2657XVFagf6w130_assertion;
    np:hasProvenance dgn-np:NP1173637.RApInDgMw956C_92IeBXQlb0ls12-e0Gr2657XVFagf6w130_provenance;
    np:hasPublicationInfo dgn-np:NP1173637.RApInDgMw956C_92IeBXQlb0ls12-e0Gr2657XVFagf6w130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1173637.RApInDgMw956C_92IeBXQlb0ls12-e0Gr2657XVFagf6w130_assertion a np:Assertion .
  
  dgn-np:NP1173637.RApInDgMw956C_92IeBXQlb0ls12-e0Gr2657XVFagf6w130_provenance a np:Provenance .
  
  dgn-np:NP1173637.RApInDgMw956C_92IeBXQlb0ls12-e0Gr2657XVFagf6w130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1173637.RApInDgMw956C_92IeBXQlb0ls12-e0Gr2657XVFagf6w130_assertion {
  miriam-gene:50506 a ncit:C16612 .
  
  lld:C0342200 a ncit:C7057 .
  
  dgn-gda:DGNf1581fd8ae69bc03ac4db26033fdf818 sio:SIO_000628 miriam-gene:50506, lld:C0342200;
    a sio:SIO_001121 .
}

dgn-np:NP1173637.RApInDgMw956C_92IeBXQlb0ls12-e0Gr2657XVFagf6w130_provenance {
  dgn-np:NP1173637.RApInDgMw956C_92IeBXQlb0ls12-e0Gr2657XVFagf6w130_assertion dcterms:description
      "[Because the relationships between DUOX2 genotypes and clinical phenotypes are extremely complex, however, further studies are needed to identify more mutations in known genes which are involved in CH and goitre.]. 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:NP1173637.RApInDgMw956C_92IeBXQlb0ls12-e0Gr2657XVFagf6w130_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" .
}