@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1364117.RATvzixxPUrbAKr4e9k4ZeJPyb76UVO8QE_Vr9BvT4hyc> .
@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:NP1364117.RATvzixxPUrbAKr4e9k4ZeJPyb76UVO8QE_Vr9BvT4hyc130_head {
   this: np:hasAssertion dgn-np:NP1364117.RATvzixxPUrbAKr4e9k4ZeJPyb76UVO8QE_Vr9BvT4hyc130_assertion ;
    np:hasProvenance dgn-np:NP1364117.RATvzixxPUrbAKr4e9k4ZeJPyb76UVO8QE_Vr9BvT4hyc130_provenance ;
    np:hasPublicationInfo dgn-np:NP1364117.RATvzixxPUrbAKr4e9k4ZeJPyb76UVO8QE_Vr9BvT4hyc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP1364117.RATvzixxPUrbAKr4e9k4ZeJPyb76UVO8QE_Vr9BvT4hyc130_assertion a np:Assertion .
  dgn-np:NP1364117.RATvzixxPUrbAKr4e9k4ZeJPyb76UVO8QE_Vr9BvT4hyc130_provenance a np:Provenance .
  dgn-np:NP1364117.RATvzixxPUrbAKr4e9k4ZeJPyb76UVO8QE_Vr9BvT4hyc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1364117.RATvzixxPUrbAKr4e9k4ZeJPyb76UVO8QE_Vr9BvT4hyc130_assertion {
   miriam-gene:10587 a ncit:C16612 .
  lld:C2940786 a ncit:C7057 .
  dgn-gda:DGN3b06ad7da655fc94177f18badea64f3d sio:SIO_000628 miriam-gene:10587 , lld:C2940786 ;
    a sio:SIO_001121 .
}
dgn-np:NP1364117.RATvzixxPUrbAKr4e9k4ZeJPyb76UVO8QE_Vr9BvT4hyc130_provenance {
   dgn-np:NP1364117.RATvzixxPUrbAKr4e9k4ZeJPyb76UVO8QE_Vr9BvT4hyc130_assertion dcterms:description "[Since similar mutations have been identified in tri-iodothyronine (T3) receptor (TR) beta gene in GRTH and PRTH, and since considerable overlap has been seen in the clinical manifestations in patients with GRTH and PRTH, two subtypes of RTH are now considered to be a continuous spectrum with the same genetic defect.]. 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:8958790 ;
    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:NP1364117.RATvzixxPUrbAKr4e9k4ZeJPyb76UVO8QE_Vr9BvT4hyc130_publicationInfo {
   this: dcterms:created "2016-05-13T12:52:04+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" .
}