@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP760527.RA6RpG-LOwTrHDnT01soAxFJqwCC2M1B3MdmrQLh2bym0> .
@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/v3.0.0/void/> .

dgn-np:NP760527.RA6RpG-LOwTrHDnT01soAxFJqwCC2M1B3MdmrQLh2bym0130_head {
  this: np:hasAssertion dgn-np:NP760527.RA6RpG-LOwTrHDnT01soAxFJqwCC2M1B3MdmrQLh2bym0130_assertion;
    np:hasProvenance dgn-np:NP760527.RA6RpG-LOwTrHDnT01soAxFJqwCC2M1B3MdmrQLh2bym0130_provenance;
    np:hasPublicationInfo dgn-np:NP760527.RA6RpG-LOwTrHDnT01soAxFJqwCC2M1B3MdmrQLh2bym0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP760527.RA6RpG-LOwTrHDnT01soAxFJqwCC2M1B3MdmrQLh2bym0130_assertion a np:Assertion .
  
  dgn-np:NP760527.RA6RpG-LOwTrHDnT01soAxFJqwCC2M1B3MdmrQLh2bym0130_provenance a np:Provenance .
  
  dgn-np:NP760527.RA6RpG-LOwTrHDnT01soAxFJqwCC2M1B3MdmrQLh2bym0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP760527.RA6RpG-LOwTrHDnT01soAxFJqwCC2M1B3MdmrQLh2bym0130_assertion {
  miriam-gene:7253 a ncit:C16612 .
  
  lld:C0018213 a ncit:C7057 .
  
  dgn-gda:DGN6f6812a15188114218013c194b19d889 sio:SIO_000628 miriam-gene:7253, lld:C0018213;
    a sio:SIO_001122 .
}

dgn-np:NP760527.RA6RpG-LOwTrHDnT01soAxFJqwCC2M1B3MdmrQLh2bym0130_provenance {
  dgn-np:NP760527.RA6RpG-LOwTrHDnT01soAxFJqwCC2M1B3MdmrQLh2bym0130_assertion dcterms:description
      "[These findings indicate that rs12101261 and rs179243 are the possible causal SNPs for GD susceptibility in the TSHR gene and could serve as genetic markers to predict the outcome of pTRAb+ in GD patients.]. 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:24144966;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP760527.RA6RpG-LOwTrHDnT01soAxFJqwCC2M1B3MdmrQLh2bym0130_publicationInfo {
  this: dcterms:created "2015-08-25T14:45:19+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}