@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP180765.RAulG-mKgaMYjNc-ZQlkdppFW2dt_hYz9GB058uurj16U> .
@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:NP180765.RAulG-mKgaMYjNc-ZQlkdppFW2dt_hYz9GB058uurj16U130_head {
  this: np:hasAssertion dgn-np:NP180765.RAulG-mKgaMYjNc-ZQlkdppFW2dt_hYz9GB058uurj16U130_assertion;
    np:hasProvenance dgn-np:NP180765.RAulG-mKgaMYjNc-ZQlkdppFW2dt_hYz9GB058uurj16U130_provenance;
    np:hasPublicationInfo dgn-np:NP180765.RAulG-mKgaMYjNc-ZQlkdppFW2dt_hYz9GB058uurj16U130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP180765.RAulG-mKgaMYjNc-ZQlkdppFW2dt_hYz9GB058uurj16U130_assertion a np:Assertion .
  
  dgn-np:NP180765.RAulG-mKgaMYjNc-ZQlkdppFW2dt_hYz9GB058uurj16U130_provenance a np:Provenance .
  
  dgn-np:NP180765.RAulG-mKgaMYjNc-ZQlkdppFW2dt_hYz9GB058uurj16U130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP180765.RAulG-mKgaMYjNc-ZQlkdppFW2dt_hYz9GB058uurj16U130_assertion {
  miriam-gene:7253 a ncit:C16612 .
  
  lld:C1836706 a ncit:C7057 .
  
  dgn-gda:DGN884a8c2bc1a93db3b695b09c544f0619 sio:SIO_000628 miriam-gene:7253, lld:C1836706;
    a sio:SIO_001121 .
}

dgn-np:NP180765.RAulG-mKgaMYjNc-ZQlkdppFW2dt_hYz9GB058uurj16U130_provenance {
  dgn-np:NP180765.RAulG-mKgaMYjNc-ZQlkdppFW2dt_hYz9GB058uurj16U130_assertion dcterms:description
      "[A review of all previously reported cases of NAH due to an activating TSHR germline mutation showed that the mean duration of gestation in these patients was significantly lower than in patients with inactivating TSHR mutations causing congenital hypothyroidism (35.8 weeks vs. 39.4 weeks, P = 0.003).]. 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:15163335;
    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:NP180765.RAulG-mKgaMYjNc-ZQlkdppFW2dt_hYz9GB058uurj16U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:38+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: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" .
}