@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP440234.RAtVqXYhifl1WD-t7kiui0ZRliHRiPy25opV31M3AhqjA> .
@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:NP440234.RAtVqXYhifl1WD-t7kiui0ZRliHRiPy25opV31M3AhqjA130_head {
  this: np:hasAssertion dgn-np:NP440234.RAtVqXYhifl1WD-t7kiui0ZRliHRiPy25opV31M3AhqjA130_assertion;
    np:hasProvenance dgn-np:NP440234.RAtVqXYhifl1WD-t7kiui0ZRliHRiPy25opV31M3AhqjA130_provenance;
    np:hasPublicationInfo dgn-np:NP440234.RAtVqXYhifl1WD-t7kiui0ZRliHRiPy25opV31M3AhqjA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP440234.RAtVqXYhifl1WD-t7kiui0ZRliHRiPy25opV31M3AhqjA130_assertion a np:Assertion .
  
  dgn-np:NP440234.RAtVqXYhifl1WD-t7kiui0ZRliHRiPy25opV31M3AhqjA130_provenance a np:Provenance .
  
  dgn-np:NP440234.RAtVqXYhifl1WD-t7kiui0ZRliHRiPy25opV31M3AhqjA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP440234.RAtVqXYhifl1WD-t7kiui0ZRliHRiPy25opV31M3AhqjA130_assertion {
  miriam-gene:7253 a ncit:C16612 .
  
  lld:C0010308 a ncit:C7057 .
  
  dgn-gda:DGN58f04e9ede02259e5f2d44ccc16c555e sio:SIO_000628 miriam-gene:7253, lld:C0010308;
    a sio:SIO_001121 .
}

dgn-np:NP440234.RAtVqXYhifl1WD-t7kiui0ZRliHRiPy25opV31M3AhqjA130_provenance {
  dgn-np:NP440234.RAtVqXYhifl1WD-t7kiui0ZRliHRiPy25opV31M3AhqjA130_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:NP440234.RAtVqXYhifl1WD-t7kiui0ZRliHRiPy25opV31M3AhqjA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:20+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" .
}