@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP98578.RAR1Zvqr8Oltw83AgMx5aikcxPD2GH2owO_ez9L6iodnw> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .
dgn-np:NP98578.RAR1Zvqr8Oltw83AgMx5aikcxPD2GH2owO_ez9L6iodnw130_head {
  this: np:hasAssertion dgn-np:NP98578.RAR1Zvqr8Oltw83AgMx5aikcxPD2GH2owO_ez9L6iodnw130_assertion ;
    np:hasProvenance dgn-np:NP98578.RAR1Zvqr8Oltw83AgMx5aikcxPD2GH2owO_ez9L6iodnw130_provenance ;
    np:hasPublicationInfo dgn-np:NP98578.RAR1Zvqr8Oltw83AgMx5aikcxPD2GH2owO_ez9L6iodnw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP98578.RAR1Zvqr8Oltw83AgMx5aikcxPD2GH2owO_ez9L6iodnw130_assertion a np:Assertion .
  dgn-np:NP98578.RAR1Zvqr8Oltw83AgMx5aikcxPD2GH2owO_ez9L6iodnw130_provenance a np:Provenance .
  dgn-np:NP98578.RAR1Zvqr8Oltw83AgMx5aikcxPD2GH2owO_ez9L6iodnw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP98578.RAR1Zvqr8Oltw83AgMx5aikcxPD2GH2owO_ez9L6iodnw130_assertion {
  miriam-gene:3576 a ncit:C16612 .
  lld:C0035328 a ncit:C7057 .
  dgn-gda:DGN0f7d63b92d33e78a71550a78658ef42f sio:SIO_000628 miriam-gene:3576 , lld:C0035328 ;
    a sio:SIO_001122 .
}
dgn-np:NP98578.RAR1Zvqr8Oltw83AgMx5aikcxPD2GH2owO_ez9L6iodnw130_provenance {
  dgn-np:NP98578.RAR1Zvqr8Oltw83AgMx5aikcxPD2GH2owO_ez9L6iodnw130_assertion dcterms:description "[As none of the investigated gene variants was significantly more prevalent in BRVO patients than among control subjects, our data suggest that these polymorphisms themselves are unlikely major risk factors for BRVO.]. 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:19347053 ;
    prov:wasDerivedFrom dgn-void:gad-20150221 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP98578.RAR1Zvqr8Oltw83AgMx5aikcxPD2GH2owO_ez9L6iodnw130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:34+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:disgenetv3.0rdf ;
    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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}