@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP165648.RAmp8r28wjPu4Ps3jUT2RHmhgKy4c9tlCX3hBdDgpHLTM> .
@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:NP165648.RAmp8r28wjPu4Ps3jUT2RHmhgKy4c9tlCX3hBdDgpHLTM130_head {
  this: np:hasAssertion dgn-np:NP165648.RAmp8r28wjPu4Ps3jUT2RHmhgKy4c9tlCX3hBdDgpHLTM130_assertion;
    np:hasProvenance dgn-np:NP165648.RAmp8r28wjPu4Ps3jUT2RHmhgKy4c9tlCX3hBdDgpHLTM130_provenance;
    np:hasPublicationInfo dgn-np:NP165648.RAmp8r28wjPu4Ps3jUT2RHmhgKy4c9tlCX3hBdDgpHLTM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP165648.RAmp8r28wjPu4Ps3jUT2RHmhgKy4c9tlCX3hBdDgpHLTM130_assertion a np:Assertion .
  
  dgn-np:NP165648.RAmp8r28wjPu4Ps3jUT2RHmhgKy4c9tlCX3hBdDgpHLTM130_provenance a np:Provenance .
  
  dgn-np:NP165648.RAmp8r28wjPu4Ps3jUT2RHmhgKy4c9tlCX3hBdDgpHLTM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP165648.RAmp8r28wjPu4Ps3jUT2RHmhgKy4c9tlCX3hBdDgpHLTM130_assertion {
  miriam-gene:7100 a ncit:C16612 .
  
  lld:C0003873 a ncit:C7057 .
  
  dgn-gda:DGNa00ddf09a45ec66a35de4d63a0ce4e26 sio:SIO_000628 miriam-gene:7100, lld:C0003873;
    a sio:SIO_001122 .
}

dgn-np:NP165648.RAmp8r28wjPu4Ps3jUT2RHmhgKy4c9tlCX3hBdDgpHLTM130_provenance {
  dgn-np:NP165648.RAmp8r28wjPu4Ps3jUT2RHmhgKy4c9tlCX3hBdDgpHLTM130_assertion dcterms:description
      "[Using a large inception cohort and strict statistical evaluation, we could not identify an association between functional TLR variants and RA phenotype and disease severity. This suggests the functional TLR variants do not play a major role in RA phenotyp]. 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:20194452;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP165648.RAmp8r28wjPu4Ps3jUT2RHmhgKy4c9tlCX3hBdDgpHLTM130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:02+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" .
}