@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP786293.RA1ynwMBGRy5VTEpdhB7TrMvrB_9HkI2TcO4mymwlnieA> .
@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:NP786293.RA1ynwMBGRy5VTEpdhB7TrMvrB_9HkI2TcO4mymwlnieA130_head {
  this: np:hasAssertion dgn-np:NP786293.RA1ynwMBGRy5VTEpdhB7TrMvrB_9HkI2TcO4mymwlnieA130_assertion ;
    np:hasProvenance dgn-np:NP786293.RA1ynwMBGRy5VTEpdhB7TrMvrB_9HkI2TcO4mymwlnieA130_provenance ;
    np:hasPublicationInfo dgn-np:NP786293.RA1ynwMBGRy5VTEpdhB7TrMvrB_9HkI2TcO4mymwlnieA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP786293.RA1ynwMBGRy5VTEpdhB7TrMvrB_9HkI2TcO4mymwlnieA130_assertion a np:Assertion .
  dgn-np:NP786293.RA1ynwMBGRy5VTEpdhB7TrMvrB_9HkI2TcO4mymwlnieA130_provenance a np:Provenance .
  dgn-np:NP786293.RA1ynwMBGRy5VTEpdhB7TrMvrB_9HkI2TcO4mymwlnieA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP786293.RA1ynwMBGRy5VTEpdhB7TrMvrB_9HkI2TcO4mymwlnieA130_assertion {
  miriam-gene:246319 a ncit:C16612 .
  lld:C0149745 a ncit:C7057 .
  dgn-gda:DGN1848257a3c099bf6eaa378c827eaba3b sio:SIO_000628 miriam-gene:246319 , lld:C0149745 ;
    a sio:SIO_001121 .
}
dgn-np:NP786293.RA1ynwMBGRy5VTEpdhB7TrMvrB_9HkI2TcO4mymwlnieA130_provenance {
  dgn-np:NP786293.RA1ynwMBGRy5VTEpdhB7TrMvrB_9HkI2TcO4mymwlnieA130_assertion dcterms:description "[Stratification analysis according to tinnitus, alopecia, poliosis, headache, and vitiligo for VKH syndrome and oral ulceration, genital ulceration, skin lesions and arthritis for BD failed to find any association between the tested single nucleotide polymorphism and any of the extraocular findings.]. 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:20438790 ;
    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:NP786293.RA1ynwMBGRy5VTEpdhB7TrMvrB_9HkI2TcO4mymwlnieA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:56+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" .
}