@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP557572.RAA9aopCbwuAHeAAOl2Zwdr5IJXxZbpAzlWlJIJlZltuc> .
@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:NP557572.RAA9aopCbwuAHeAAOl2Zwdr5IJXxZbpAzlWlJIJlZltuc130_head {
  this: np:hasAssertion dgn-np:NP557572.RAA9aopCbwuAHeAAOl2Zwdr5IJXxZbpAzlWlJIJlZltuc130_assertion;
    np:hasProvenance dgn-np:NP557572.RAA9aopCbwuAHeAAOl2Zwdr5IJXxZbpAzlWlJIJlZltuc130_provenance;
    np:hasPublicationInfo dgn-np:NP557572.RAA9aopCbwuAHeAAOl2Zwdr5IJXxZbpAzlWlJIJlZltuc130_publicationInfo;
    a np:Nanopublication .
  
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  dgn-np:NP557572.RAA9aopCbwuAHeAAOl2Zwdr5IJXxZbpAzlWlJIJlZltuc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP557572.RAA9aopCbwuAHeAAOl2Zwdr5IJXxZbpAzlWlJIJlZltuc130_assertion {
  miriam-gene:26191 a ncit:C16612 .
  
  lld:C0036421 a ncit:C7057 .
  
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dgn-np:NP557572.RAA9aopCbwuAHeAAOl2Zwdr5IJXxZbpAzlWlJIJlZltuc130_provenance {
  dgn-np:NP557572.RAA9aopCbwuAHeAAOl2Zwdr5IJXxZbpAzlWlJIJlZltuc130_assertion dcterms:description
      "[The association of subsets of SSc with the PTPN22 R620W polymorphism further strengthens the classification of SSc within the spectrum of autoimmune diseases and strongly suggests the involvement of common susceptibility genes and similarly disordered immunoregulatory pathways.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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    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:NP557572.RAA9aopCbwuAHeAAOl2Zwdr5IJXxZbpAzlWlJIJlZltuc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:36+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;
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  dgn-void:disgenetrdf pav:version "v2.1.0" .
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