@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP493867.RAhdSvetp5jF-SnJyFR2zkvC7Aoq7-RfdMhFhAelFhscc> .
@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:NP493867.RAhdSvetp5jF-SnJyFR2zkvC7Aoq7-RfdMhFhAelFhscc130_head {
  this: np:hasAssertion dgn-np:NP493867.RAhdSvetp5jF-SnJyFR2zkvC7Aoq7-RfdMhFhAelFhscc130_assertion ;
    np:hasProvenance dgn-np:NP493867.RAhdSvetp5jF-SnJyFR2zkvC7Aoq7-RfdMhFhAelFhscc130_provenance ;
    np:hasPublicationInfo dgn-np:NP493867.RAhdSvetp5jF-SnJyFR2zkvC7Aoq7-RfdMhFhAelFhscc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP493867.RAhdSvetp5jF-SnJyFR2zkvC7Aoq7-RfdMhFhAelFhscc130_assertion a np:Assertion .
  dgn-np:NP493867.RAhdSvetp5jF-SnJyFR2zkvC7Aoq7-RfdMhFhAelFhscc130_provenance a np:Provenance .
  dgn-np:NP493867.RAhdSvetp5jF-SnJyFR2zkvC7Aoq7-RfdMhFhAelFhscc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP493867.RAhdSvetp5jF-SnJyFR2zkvC7Aoq7-RfdMhFhAelFhscc130_assertion {
  miriam-gene:5698 a ncit:C16612 .
  lld:C0038013 a ncit:C7057 .
  dgn-gda:DGN4261d2b2d33af25fde4fdd87e1aeef4d sio:SIO_000628 miriam-gene:5698 , lld:C0038013 ;
    a sio:SIO_001121 .
}
dgn-np:NP493867.RAhdSvetp5jF-SnJyFR2zkvC7Aoq7-RfdMhFhAelFhscc130_provenance {
  dgn-np:NP493867.RAhdSvetp5jF-SnJyFR2zkvC7Aoq7-RfdMhFhAelFhscc130_assertion dcterms:description "[A polymorphic CfoI restriction enzyme site in the coding region of the LMP2 gene was evaluated in genomic DNA samples from 193 white and 49 Chinese B27 individuals with well documented AS, 97 of whom had had acute anterior uveitis (AAU) and 97 peripheral arthritis; 42 samples from normal, white, B27 positive blood donors in whom AS was excluded were also evaluated.]. 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:7763114 ;
    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:NP493867.RAhdSvetp5jF-SnJyFR2zkvC7Aoq7-RfdMhFhAelFhscc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:55+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" .
}