@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP665369.RAdpnD5isgIvS4Me0jNTC-gfGfack5PeOx0NndSCysvEk> .
@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:NP665369.RAdpnD5isgIvS4Me0jNTC-gfGfack5PeOx0NndSCysvEk130_head {
  this: np:hasAssertion dgn-np:NP665369.RAdpnD5isgIvS4Me0jNTC-gfGfack5PeOx0NndSCysvEk130_assertion ;
    np:hasProvenance dgn-np:NP665369.RAdpnD5isgIvS4Me0jNTC-gfGfack5PeOx0NndSCysvEk130_provenance ;
    np:hasPublicationInfo dgn-np:NP665369.RAdpnD5isgIvS4Me0jNTC-gfGfack5PeOx0NndSCysvEk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP665369.RAdpnD5isgIvS4Me0jNTC-gfGfack5PeOx0NndSCysvEk130_assertion a np:Assertion .
  dgn-np:NP665369.RAdpnD5isgIvS4Me0jNTC-gfGfack5PeOx0NndSCysvEk130_provenance a np:Provenance .
  dgn-np:NP665369.RAdpnD5isgIvS4Me0jNTC-gfGfack5PeOx0NndSCysvEk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP665369.RAdpnD5isgIvS4Me0jNTC-gfGfack5PeOx0NndSCysvEk130_assertion {
  miriam-gene:3106 a ncit:C16612 .
  lld:C0035435 a ncit:C7057 .
  dgn-gda:DGN5b76149d09dc15e8e88ab8eef9a7d50b sio:SIO_000628 miriam-gene:3106 , lld:C0035435 ;
    a sio:SIO_001121 .
}
dgn-np:NP665369.RAdpnD5isgIvS4Me0jNTC-gfGfack5PeOx0NndSCysvEk130_provenance {
  dgn-np:NP665369.RAdpnD5isgIvS4Me0jNTC-gfGfack5PeOx0NndSCysvEk130_assertion dcterms:description "[To test the pathogenetic role of the phenotype MZ of alpha 1-antitrypsin/alpha 1-protease inhibitor (PI) in acute anterior uveitis (AAU) and in different rheumatic diseases we examined 360 unrelated patients including 93 with AAU alone, 24 patients with AAU and ankylosing spondylitis (AS), 21 patients with AAU and Reiter's disease (RD), 26 patients with AAU, AS, and RD 54 patients with AS alone, 16 patients with RD alone, 115 patients with rheumatoid arthritis (RA) alone, and 11 patients with psoriatic arthritis (PA) alone.]. 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 ;
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  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:NP665369.RAdpnD5isgIvS4Me0jNTC-gfGfack5PeOx0NndSCysvEk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:42+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> ;
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}