@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP50855.RAYp34tXg3UpUvRWkdnExAKKVotdnPV-VU9wq7pAv0oTM> .
@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:NP50855.RAYp34tXg3UpUvRWkdnExAKKVotdnPV-VU9wq7pAv0oTM130_head {
  this: np:hasAssertion dgn-np:NP50855.RAYp34tXg3UpUvRWkdnExAKKVotdnPV-VU9wq7pAv0oTM130_assertion ;
    np:hasProvenance dgn-np:NP50855.RAYp34tXg3UpUvRWkdnExAKKVotdnPV-VU9wq7pAv0oTM130_provenance ;
    np:hasPublicationInfo dgn-np:NP50855.RAYp34tXg3UpUvRWkdnExAKKVotdnPV-VU9wq7pAv0oTM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP50855.RAYp34tXg3UpUvRWkdnExAKKVotdnPV-VU9wq7pAv0oTM130_assertion a np:Assertion .
  dgn-np:NP50855.RAYp34tXg3UpUvRWkdnExAKKVotdnPV-VU9wq7pAv0oTM130_provenance a np:Provenance .
  dgn-np:NP50855.RAYp34tXg3UpUvRWkdnExAKKVotdnPV-VU9wq7pAv0oTM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP50855.RAYp34tXg3UpUvRWkdnExAKKVotdnPV-VU9wq7pAv0oTM130_assertion {
  miriam-gene:6891 a ncit:C16612 .
  lld:C0003873 a ncit:C7057 .
  dgn-gda:DGN804bf5d018e706e485f7963a8a936352 sio:SIO_000628 miriam-gene:6891 , lld:C0003873 ;
    a sio:SIO_001122 .
}
dgn-np:NP50855.RAYp34tXg3UpUvRWkdnExAKKVotdnPV-VU9wq7pAv0oTM130_provenance {
  dgn-np:NP50855.RAYp34tXg3UpUvRWkdnExAKKVotdnPV-VU9wq7pAv0oTM130_assertion dcterms:description "[We concluded that the TAP2 gene codon 565 'A' allele was associated with RA in Chinese patients in Taiwan. Individuals possessing the 'A' allele had a higher incidence of RA. A lack of association of TAP1 gene polymorphisms between RA patients and healthy individuals was noted. The results of this study provide genetic evidence that TAP2 gene codon 565 polymorphism may play a role in RA.]. 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:14749980 ;
    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:NP50855.RAYp34tXg3UpUvRWkdnExAKKVotdnPV-VU9wq7pAv0oTM130_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" .
}