@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP585149.RAOTDNi1hLHkoKg9Kkjnrz5tuCc49K0iZSFPGW_JJcCu8> .
@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:NP585149.RAOTDNi1hLHkoKg9Kkjnrz5tuCc49K0iZSFPGW_JJcCu8130_head {
  this: np:hasAssertion dgn-np:NP585149.RAOTDNi1hLHkoKg9Kkjnrz5tuCc49K0iZSFPGW_JJcCu8130_assertion ;
    np:hasProvenance dgn-np:NP585149.RAOTDNi1hLHkoKg9Kkjnrz5tuCc49K0iZSFPGW_JJcCu8130_provenance ;
    np:hasPublicationInfo dgn-np:NP585149.RAOTDNi1hLHkoKg9Kkjnrz5tuCc49K0iZSFPGW_JJcCu8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP585149.RAOTDNi1hLHkoKg9Kkjnrz5tuCc49K0iZSFPGW_JJcCu8130_assertion a np:Assertion .
  dgn-np:NP585149.RAOTDNi1hLHkoKg9Kkjnrz5tuCc49K0iZSFPGW_JJcCu8130_provenance a np:Provenance .
  dgn-np:NP585149.RAOTDNi1hLHkoKg9Kkjnrz5tuCc49K0iZSFPGW_JJcCu8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP585149.RAOTDNi1hLHkoKg9Kkjnrz5tuCc49K0iZSFPGW_JJcCu8130_assertion {
  miriam-gene:3133 a ncit:C16612 .
  lld:C0701807 a ncit:C7057 .
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    a sio:SIO_001121 .
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dgn-np:NP585149.RAOTDNi1hLHkoKg9Kkjnrz5tuCc49K0iZSFPGW_JJcCu8130_provenance {
  dgn-np:NP585149.RAOTDNi1hLHkoKg9Kkjnrz5tuCc49K0iZSFPGW_JJcCu8130_assertion dcterms:description "[In the absence of evidence of linkage disequilibrium between A2 and B27 in the general population, the data suggest that the presence of A2 in B27 positive AS patients enhances the risk of AAU above that associated with B27 alone, and that other MHC-linked genetic factors, in addition to B27, are associated with susceptibility to AAU in AS patients.]. 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 ;
    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 .
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dgn-np:NP585149.RAOTDNi1hLHkoKg9Kkjnrz5tuCc49K0iZSFPGW_JJcCu8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:52+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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