@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP788673.RATlYrly1lMDyDCuJhu3j4RGRuuak5iWPh-xi4iGPhdvU> .
@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:NP788673.RATlYrly1lMDyDCuJhu3j4RGRuuak5iWPh-xi4iGPhdvU130_head {
  this: np:hasAssertion dgn-np:NP788673.RATlYrly1lMDyDCuJhu3j4RGRuuak5iWPh-xi4iGPhdvU130_assertion ;
    np:hasProvenance dgn-np:NP788673.RATlYrly1lMDyDCuJhu3j4RGRuuak5iWPh-xi4iGPhdvU130_provenance ;
    np:hasPublicationInfo dgn-np:NP788673.RATlYrly1lMDyDCuJhu3j4RGRuuak5iWPh-xi4iGPhdvU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP788673.RATlYrly1lMDyDCuJhu3j4RGRuuak5iWPh-xi4iGPhdvU130_assertion a np:Assertion .
  dgn-np:NP788673.RATlYrly1lMDyDCuJhu3j4RGRuuak5iWPh-xi4iGPhdvU130_provenance a np:Provenance .
  dgn-np:NP788673.RATlYrly1lMDyDCuJhu3j4RGRuuak5iWPh-xi4iGPhdvU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP788673.RATlYrly1lMDyDCuJhu3j4RGRuuak5iWPh-xi4iGPhdvU130_assertion {
  miriam-gene:7038 a ncit:C16612 .
  lld:C0349476 a ncit:C7057 .
  dgn-gda:DGN9a8c05c3a2c499435dcd42d11f1bd41c sio:SIO_000628 miriam-gene:7038 , lld:C0349476 ;
    a sio:SIO_001121 .
}
dgn-np:NP788673.RATlYrly1lMDyDCuJhu3j4RGRuuak5iWPh-xi4iGPhdvU130_provenance {
  dgn-np:NP788673.RATlYrly1lMDyDCuJhu3j4RGRuuak5iWPh-xi4iGPhdvU130_assertion dcterms:description "[This dyshormonogenesis displays a wide phenotype variation and is characterized usually by: the presence of congenital goiter or goiter appearing shortly after birth, high (131)I uptake, negative perchlorate discharge test, low serum TG and elevated serum TSH with simultaneous low serum T(4) and low, normal or high serum T(3).]. 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:20093166 ;
    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:NP788673.RATlYrly1lMDyDCuJhu3j4RGRuuak5iWPh-xi4iGPhdvU130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:42+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" .
}