@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP747571.RAonzDOaCtZBCJUKM_9TOtTmvJ0BlQDSUm1CL53Ia2bZ8> .
@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:NP747571.RAonzDOaCtZBCJUKM_9TOtTmvJ0BlQDSUm1CL53Ia2bZ8130_head {
  this: np:hasAssertion dgn-np:NP747571.RAonzDOaCtZBCJUKM_9TOtTmvJ0BlQDSUm1CL53Ia2bZ8130_assertion;
    np:hasProvenance dgn-np:NP747571.RAonzDOaCtZBCJUKM_9TOtTmvJ0BlQDSUm1CL53Ia2bZ8130_provenance;
    np:hasPublicationInfo dgn-np:NP747571.RAonzDOaCtZBCJUKM_9TOtTmvJ0BlQDSUm1CL53Ia2bZ8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP747571.RAonzDOaCtZBCJUKM_9TOtTmvJ0BlQDSUm1CL53Ia2bZ8130_assertion a np:Assertion .
  
  dgn-np:NP747571.RAonzDOaCtZBCJUKM_9TOtTmvJ0BlQDSUm1CL53Ia2bZ8130_provenance a np:Provenance .
  
  dgn-np:NP747571.RAonzDOaCtZBCJUKM_9TOtTmvJ0BlQDSUm1CL53Ia2bZ8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP747571.RAonzDOaCtZBCJUKM_9TOtTmvJ0BlQDSUm1CL53Ia2bZ8130_assertion {
  miriam-gene:26191 a ncit:C16612 .
  
  lld:C0015397 a ncit:C7057 .
  
  dgn-gda:DGN8434f29d0a9122306de435cb42a03fce sio:SIO_000628 miriam-gene:26191, lld:C0015397;
    a sio:SIO_001121 .
}

dgn-np:NP747571.RAonzDOaCtZBCJUKM_9TOtTmvJ0BlQDSUm1CL53Ia2bZ8130_provenance {
  dgn-np:NP747571.RAonzDOaCtZBCJUKM_9TOtTmvJ0BlQDSUm1CL53Ia2bZ8130_assertion dcterms:description
      "[No other statistically significant associations between the ESR2 genotype and GD subsets were found (age of onset, smoking, clinically evident ophthalmopathy, family history of GD, and PTPN22 and CTLA4 (CT60) genotypes were analysed).]. 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:17941906;
    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:NP747571.RAonzDOaCtZBCJUKM_9TOtTmvJ0BlQDSUm1CL53Ia2bZ8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:33+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}