@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP58871.RAjDTNUhrPxH4GRwxi7-DRwF1beNHtw6rZh4N8ocOYHZw> .
@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:NP58871.RAjDTNUhrPxH4GRwxi7-DRwF1beNHtw6rZh4N8ocOYHZw130_head {
  this: np:hasAssertion dgn-np:NP58871.RAjDTNUhrPxH4GRwxi7-DRwF1beNHtw6rZh4N8ocOYHZw130_assertion;
    np:hasProvenance dgn-np:NP58871.RAjDTNUhrPxH4GRwxi7-DRwF1beNHtw6rZh4N8ocOYHZw130_provenance;
    np:hasPublicationInfo dgn-np:NP58871.RAjDTNUhrPxH4GRwxi7-DRwF1beNHtw6rZh4N8ocOYHZw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP58871.RAjDTNUhrPxH4GRwxi7-DRwF1beNHtw6rZh4N8ocOYHZw130_assertion a np:Assertion .
  
  dgn-np:NP58871.RAjDTNUhrPxH4GRwxi7-DRwF1beNHtw6rZh4N8ocOYHZw130_provenance a np:Provenance .
  
  dgn-np:NP58871.RAjDTNUhrPxH4GRwxi7-DRwF1beNHtw6rZh4N8ocOYHZw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP58871.RAjDTNUhrPxH4GRwxi7-DRwF1beNHtw6rZh4N8ocOYHZw130_assertion {
  miriam-gene:7253 a ncit:C16612 .
  
  lld:C0018213 a ncit:C7057 .
  
  dgn-gda:DGN82cbe2139d712dda8eabe7f9e5609c9e sio:SIO_000628 miriam-gene:7253, lld:C0018213;
    a sio:SIO_001122 .
}

dgn-np:NP58871.RAjDTNUhrPxH4GRwxi7-DRwF1beNHtw6rZh4N8ocOYHZw130_provenance {
  dgn-np:NP58871.RAjDTNUhrPxH4GRwxi7-DRwF1beNHtw6rZh4N8ocOYHZw130_assertion dcterms:description
      "[Together with recent identification of disease susceptibility markers in the region of the TSHr gene, these results are supportive of genetic factors existing in this region that may be in linkage disequilibrium with the inheritance of various TSHr polymorphisms.]. 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:12930595;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP58871.RAjDTNUhrPxH4GRwxi7-DRwF1beNHtw6rZh4N8ocOYHZw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:27+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" .
}