@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP464353.RAi0VmfGTZCTSITnCtQSNc0J7KnnAs05gfJEl4IR9K9HU> .
@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:NP464353.RAi0VmfGTZCTSITnCtQSNc0J7KnnAs05gfJEl4IR9K9HU130_head {
   this: np:hasAssertion dgn-np:NP464353.RAi0VmfGTZCTSITnCtQSNc0J7KnnAs05gfJEl4IR9K9HU130_assertion ;
    np:hasProvenance dgn-np:NP464353.RAi0VmfGTZCTSITnCtQSNc0J7KnnAs05gfJEl4IR9K9HU130_provenance ;
    np:hasPublicationInfo dgn-np:NP464353.RAi0VmfGTZCTSITnCtQSNc0J7KnnAs05gfJEl4IR9K9HU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP464353.RAi0VmfGTZCTSITnCtQSNc0J7KnnAs05gfJEl4IR9K9HU130_assertion a np:Assertion .
  dgn-np:NP464353.RAi0VmfGTZCTSITnCtQSNc0J7KnnAs05gfJEl4IR9K9HU130_provenance a np:Provenance .
  dgn-np:NP464353.RAi0VmfGTZCTSITnCtQSNc0J7KnnAs05gfJEl4IR9K9HU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP464353.RAi0VmfGTZCTSITnCtQSNc0J7KnnAs05gfJEl4IR9K9HU130_assertion {
   miriam-gene:1211 a ncit:C16612 .
  lld:C0456909 a ncit:C7057 .
  dgn-gda:DGN16519b50b0d8b23ca068bdb542df4276 sio:SIO_000628 miriam-gene:1211 , lld:C0456909 ;
    a sio:SIO_001121 .
}
dgn-np:NP464353.RAi0VmfGTZCTSITnCtQSNc0J7KnnAs05gfJEl4IR9K9HU130_provenance {
   dgn-np:NP464353.RAi0VmfGTZCTSITnCtQSNc0J7KnnAs05gfJEl4IR9K9HU130_assertion dcterms:description "[These preclinical studies have already allowed the field to reach the point where gene therapy to treat inherited blindness has been brought to clinical trial.In this chapter, we focus on AAV-mediated specific gene therapy for inherited retinal degenerative diseases, describing the disease targets, the preclinical studies in animal models and the recent success of the LCA-RPE65 clinical trials.]. 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:22034031 ;
    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:NP464353.RAi0VmfGTZCTSITnCtQSNc0J7KnnAs05gfJEl4IR9K9HU130_publicationInfo {
   this: dcterms:created "2014-10-02T12:36:36+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" .
}