@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP100633.RAa9UM270A0o6R-7pp22b3d5pH2lY5KwJwmdYRgaAS0cY> .
@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:NP100633.RAa9UM270A0o6R-7pp22b3d5pH2lY5KwJwmdYRgaAS0cY130_head {
  this: np:hasAssertion dgn-np:NP100633.RAa9UM270A0o6R-7pp22b3d5pH2lY5KwJwmdYRgaAS0cY130_assertion ;
    np:hasProvenance dgn-np:NP100633.RAa9UM270A0o6R-7pp22b3d5pH2lY5KwJwmdYRgaAS0cY130_provenance ;
    np:hasPublicationInfo dgn-np:NP100633.RAa9UM270A0o6R-7pp22b3d5pH2lY5KwJwmdYRgaAS0cY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP100633.RAa9UM270A0o6R-7pp22b3d5pH2lY5KwJwmdYRgaAS0cY130_assertion a np:Assertion .
  dgn-np:NP100633.RAa9UM270A0o6R-7pp22b3d5pH2lY5KwJwmdYRgaAS0cY130_provenance a np:Provenance .
  dgn-np:NP100633.RAa9UM270A0o6R-7pp22b3d5pH2lY5KwJwmdYRgaAS0cY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP100633.RAa9UM270A0o6R-7pp22b3d5pH2lY5KwJwmdYRgaAS0cY130_assertion {
  miriam-gene:3606 a ncit:C16612 .
  lld:C0021368 a ncit:C7057 .
  dgn-gda:DGNf4eaaeb7a8566e9b7c78bc8d6b628e40 sio:SIO_000628 miriam-gene:3606 , lld:C0021368 ;
    a sio:SIO_001122 .
}
dgn-np:NP100633.RAa9UM270A0o6R-7pp22b3d5pH2lY5KwJwmdYRgaAS0cY130_provenance {
  dgn-np:NP100633.RAa9UM270A0o6R-7pp22b3d5pH2lY5KwJwmdYRgaAS0cY130_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:NP100633.RAa9UM270A0o6R-7pp22b3d5pH2lY5KwJwmdYRgaAS0cY130_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" .
}