@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP299060.RAEgah_HquUgsrdDzve2gFlhxvXXwSAWM3fSA8uT4iJvc> .
@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:NP299060.RAEgah_HquUgsrdDzve2gFlhxvXXwSAWM3fSA8uT4iJvc130_head {
  this: np:hasAssertion dgn-np:NP299060.RAEgah_HquUgsrdDzve2gFlhxvXXwSAWM3fSA8uT4iJvc130_assertion ;
    np:hasProvenance dgn-np:NP299060.RAEgah_HquUgsrdDzve2gFlhxvXXwSAWM3fSA8uT4iJvc130_provenance ;
    np:hasPublicationInfo dgn-np:NP299060.RAEgah_HquUgsrdDzve2gFlhxvXXwSAWM3fSA8uT4iJvc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP299060.RAEgah_HquUgsrdDzve2gFlhxvXXwSAWM3fSA8uT4iJvc130_assertion a np:Assertion .
  dgn-np:NP299060.RAEgah_HquUgsrdDzve2gFlhxvXXwSAWM3fSA8uT4iJvc130_provenance a np:Provenance .
  dgn-np:NP299060.RAEgah_HquUgsrdDzve2gFlhxvXXwSAWM3fSA8uT4iJvc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP299060.RAEgah_HquUgsrdDzve2gFlhxvXXwSAWM3fSA8uT4iJvc130_assertion {
  miriam-gene:29980 a ncit:C16612 .
  lld:C0033860 a ncit:C7057 .
  dgn-gda:DGN4b220c4b6dc3923c718c9ea0a0e72fdf sio:SIO_000628 miriam-gene:29980 , lld:C0033860 ;
    a sio:SIO_001121 .
}
dgn-np:NP299060.RAEgah_HquUgsrdDzve2gFlhxvXXwSAWM3fSA8uT4iJvc130_provenance {
  dgn-np:NP299060.RAEgah_HquUgsrdDzve2gFlhxvXXwSAWM3fSA8uT4iJvc130_assertion dcterms:description "[When these new findings are added to the previous observations that acute anterior uveitis probably is a clinical, sex-influenced characteristic of HLA B27 positive Bechterew's syndrome, that HLA B27 negative patients with Bechterew's syndrome frequently had psoriasis and were HLA B13 and B17 negative, and that psoriasis was frequent in HLA B27 positive patients as well, we tentatively conclude that different and interacting genetic mechanisms may be involved in the etiology of Bechterew's syndrome.]. 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:6983935 ;
    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:NP299060.RAEgah_HquUgsrdDzve2gFlhxvXXwSAWM3fSA8uT4iJvc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:50+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" .
}