@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP313124.RAVrNNrDwmLyWMuQyGF0oowaj-2kaz9rj3XNR7pMUeV3M> .
@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:NP313124.RAVrNNrDwmLyWMuQyGF0oowaj-2kaz9rj3XNR7pMUeV3M130_head {
  this: np:hasAssertion dgn-np:NP313124.RAVrNNrDwmLyWMuQyGF0oowaj-2kaz9rj3XNR7pMUeV3M130_assertion;
    np:hasProvenance dgn-np:NP313124.RAVrNNrDwmLyWMuQyGF0oowaj-2kaz9rj3XNR7pMUeV3M130_provenance;
    np:hasPublicationInfo dgn-np:NP313124.RAVrNNrDwmLyWMuQyGF0oowaj-2kaz9rj3XNR7pMUeV3M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP313124.RAVrNNrDwmLyWMuQyGF0oowaj-2kaz9rj3XNR7pMUeV3M130_assertion a np:Assertion .
  
  dgn-np:NP313124.RAVrNNrDwmLyWMuQyGF0oowaj-2kaz9rj3XNR7pMUeV3M130_provenance a np:Provenance .
  
  dgn-np:NP313124.RAVrNNrDwmLyWMuQyGF0oowaj-2kaz9rj3XNR7pMUeV3M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP313124.RAVrNNrDwmLyWMuQyGF0oowaj-2kaz9rj3XNR7pMUeV3M130_assertion {
  miriam-gene:1791 a ncit:C16612 .
  
  lld:C0003873 a ncit:C7057 .
  
  dgn-gda:DGN476944a4062f717407f5096e01f98e81 sio:SIO_000628 miriam-gene:1791, lld:C0003873;
    a sio:SIO_001121 .
}

dgn-np:NP313124.RAVrNNrDwmLyWMuQyGF0oowaj-2kaz9rj3XNR7pMUeV3M130_provenance {
  dgn-np:NP313124.RAVrNNrDwmLyWMuQyGF0oowaj-2kaz9rj3XNR7pMUeV3M130_assertion dcterms:description
      "[When the data were stratified by the presence of the SE with further stratification according to SE DR subtypes and analysed by transmission disequilibrium test (TDT) for which offspring were assumed independent, the -308A and -857T alleles were found to be associated with RA in patients carrying the SE (P = 0.0076 and 0.0063 respectively).]. 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:11393661;
    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:NP313124.RAVrNNrDwmLyWMuQyGF0oowaj-2kaz9rj3XNR7pMUeV3M130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:59+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" .
}