@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP99350.RAe49x1m04qGwB590DbZBQr24gFi7RID2wk30VuTzujH4> .
@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:NP99350.RAe49x1m04qGwB590DbZBQr24gFi7RID2wk30VuTzujH4130_head {
  this: np:hasAssertion dgn-np:NP99350.RAe49x1m04qGwB590DbZBQr24gFi7RID2wk30VuTzujH4130_assertion ;
    np:hasProvenance dgn-np:NP99350.RAe49x1m04qGwB590DbZBQr24gFi7RID2wk30VuTzujH4130_provenance ;
    np:hasPublicationInfo dgn-np:NP99350.RAe49x1m04qGwB590DbZBQr24gFi7RID2wk30VuTzujH4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP99350.RAe49x1m04qGwB590DbZBQr24gFi7RID2wk30VuTzujH4130_assertion a np:Assertion .
  dgn-np:NP99350.RAe49x1m04qGwB590DbZBQr24gFi7RID2wk30VuTzujH4130_provenance a np:Provenance .
  dgn-np:NP99350.RAe49x1m04qGwB590DbZBQr24gFi7RID2wk30VuTzujH4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP99350.RAe49x1m04qGwB590DbZBQr24gFi7RID2wk30VuTzujH4130_assertion {
  miriam-gene:3565 a ncit:C16612 .
  lld:C0035328 a ncit:C7057 .
  dgn-gda:DGNce4cfcea8d646df6203882fd5f2dda85 sio:SIO_000628 miriam-gene:3565 , lld:C0035328 ;
    a sio:SIO_001122 .
}
dgn-np:NP99350.RAe49x1m04qGwB590DbZBQr24gFi7RID2wk30VuTzujH4130_provenance {
  dgn-np:NP99350.RAe49x1m04qGwB590DbZBQr24gFi7RID2wk30VuTzujH4130_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:NP99350.RAe49x1m04qGwB590DbZBQr24gFi7RID2wk30VuTzujH4130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:35+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" .
}