@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP50614.RABJVav4AI1UIqMh_-VCtTtFk-e4t-ve7fNQQF8ulxSCc> .
@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:NP50614.RABJVav4AI1UIqMh_-VCtTtFk-e4t-ve7fNQQF8ulxSCc130_head {
  this: np:hasAssertion dgn-np:NP50614.RABJVav4AI1UIqMh_-VCtTtFk-e4t-ve7fNQQF8ulxSCc130_assertion;
    np:hasProvenance dgn-np:NP50614.RABJVav4AI1UIqMh_-VCtTtFk-e4t-ve7fNQQF8ulxSCc130_provenance;
    np:hasPublicationInfo dgn-np:NP50614.RABJVav4AI1UIqMh_-VCtTtFk-e4t-ve7fNQQF8ulxSCc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP50614.RABJVav4AI1UIqMh_-VCtTtFk-e4t-ve7fNQQF8ulxSCc130_assertion a np:Assertion .
  
  dgn-np:NP50614.RABJVav4AI1UIqMh_-VCtTtFk-e4t-ve7fNQQF8ulxSCc130_provenance a np:Provenance .
  
  dgn-np:NP50614.RABJVav4AI1UIqMh_-VCtTtFk-e4t-ve7fNQQF8ulxSCc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP50614.RABJVav4AI1UIqMh_-VCtTtFk-e4t-ve7fNQQF8ulxSCc130_assertion {
  miriam-gene:7040 a ncit:C16612 .
  
  lld:C0026769 a ncit:C7057 .
  
  dgn-gda:DGNdde7cbd273108bb902ed4ef797f0806a sio:SIO_000628 miriam-gene:7040, lld:C0026769;
    a sio:SIO_001122 .
}

dgn-np:NP50614.RABJVav4AI1UIqMh_-VCtTtFk-e4t-ve7fNQQF8ulxSCc130_provenance {
  dgn-np:NP50614.RABJVav4AI1UIqMh_-VCtTtFk-e4t-ve7fNQQF8ulxSCc130_assertion dcterms:description
      "[These results represent an independent validation of MS association with DRB1*15(2) and TNFa9 in Russians and are the first to find the interplay of three loci in conferring susceptibility to MS. They demonstrate the efficacy of our approach for the identification of complex-disease-associated combinations of alleles.]. 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:16872485;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP50614.RABJVav4AI1UIqMh_-VCtTtFk-e4t-ve7fNQQF8ulxSCc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:23+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" .
}