@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP188774.RAaBACRH-k7Xlm3ebf4eOVUW1O2bNtoIy8Ml0vNvASbtQ> .
@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:NP188774.RAaBACRH-k7Xlm3ebf4eOVUW1O2bNtoIy8Ml0vNvASbtQ130_head {
  this: np:hasAssertion dgn-np:NP188774.RAaBACRH-k7Xlm3ebf4eOVUW1O2bNtoIy8Ml0vNvASbtQ130_assertion;
    np:hasProvenance dgn-np:NP188774.RAaBACRH-k7Xlm3ebf4eOVUW1O2bNtoIy8Ml0vNvASbtQ130_provenance;
    np:hasPublicationInfo dgn-np:NP188774.RAaBACRH-k7Xlm3ebf4eOVUW1O2bNtoIy8Ml0vNvASbtQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP188774.RAaBACRH-k7Xlm3ebf4eOVUW1O2bNtoIy8Ml0vNvASbtQ130_assertion a np:Assertion .
  
  dgn-np:NP188774.RAaBACRH-k7Xlm3ebf4eOVUW1O2bNtoIy8Ml0vNvASbtQ130_provenance a np:Provenance .
  
  dgn-np:NP188774.RAaBACRH-k7Xlm3ebf4eOVUW1O2bNtoIy8Ml0vNvASbtQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP188774.RAaBACRH-k7Xlm3ebf4eOVUW1O2bNtoIy8Ml0vNvASbtQ130_assertion {
  miriam-gene:727 a ncit:C16612 .
  
  lld:C0003873 a ncit:C7057 .
  
  dgn-gda:DGN294ec7955eb3d2f204ed84d6338036f9 sio:SIO_000628 miriam-gene:727, lld:C0003873;
    a sio:SIO_001122 .
}

dgn-np:NP188774.RAaBACRH-k7Xlm3ebf4eOVUW1O2bNtoIy8Ml0vNvASbtQ130_provenance {
  dgn-np:NP188774.RAaBACRH-k7Xlm3ebf4eOVUW1O2bNtoIy8Ml0vNvASbtQ130_assertion dcterms:description
      "[The majority of RA risk alleles previously validated for RA patients of European ancestry showed similar ORs in our population of African Americans with RA. Furthermore, the aggregate GRS supports the hypothesis that these SNPs are risk alleles for RA in ]. 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:21120996;
    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:NP188774.RAaBACRH-k7Xlm3ebf4eOVUW1O2bNtoIy8Ml0vNvASbtQ130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:12+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" .
}