@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP931876.RA5f-KLOu_JBL39Z_yse6fYbR39rj5KbKaDGD7dhjFIvM> .
@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:NP931876.RA5f-KLOu_JBL39Z_yse6fYbR39rj5KbKaDGD7dhjFIvM130_head {
  this: np:hasAssertion dgn-np:NP931876.RA5f-KLOu_JBL39Z_yse6fYbR39rj5KbKaDGD7dhjFIvM130_assertion;
    np:hasProvenance dgn-np:NP931876.RA5f-KLOu_JBL39Z_yse6fYbR39rj5KbKaDGD7dhjFIvM130_provenance;
    np:hasPublicationInfo dgn-np:NP931876.RA5f-KLOu_JBL39Z_yse6fYbR39rj5KbKaDGD7dhjFIvM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP931876.RA5f-KLOu_JBL39Z_yse6fYbR39rj5KbKaDGD7dhjFIvM130_assertion a np:Assertion .
  
  dgn-np:NP931876.RA5f-KLOu_JBL39Z_yse6fYbR39rj5KbKaDGD7dhjFIvM130_provenance a np:Provenance .
  
  dgn-np:NP931876.RA5f-KLOu_JBL39Z_yse6fYbR39rj5KbKaDGD7dhjFIvM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP931876.RA5f-KLOu_JBL39Z_yse6fYbR39rj5KbKaDGD7dhjFIvM130_assertion {
  miriam-gene:5362 a ncit:C16612 .
  
  lld:C3276549 a ncit:C7057 .
  
  dgn-gda:DGNe4c481d3f5e6640d07f8507241fa48df sio:SIO_000628 miriam-gene:5362, lld:C3276549;
    a sio:SIO_001121 .
}

dgn-np:NP931876.RA5f-KLOu_JBL39Z_yse6fYbR39rj5KbKaDGD7dhjFIvM130_provenance {
  dgn-np:NP931876.RA5f-KLOu_JBL39Z_yse6fYbR39rj5KbKaDGD7dhjFIvM130_assertion dcterms:description
      "[In this prospective, observational case series, optical coherence tomography (OCT) was used to define the pattern of retinal nerve fibre layer (RNFL) loss in patients with both the pure and syndromal forms of DOA.]. 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:21378995;
    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:NP931876.RA5f-KLOu_JBL39Z_yse6fYbR39rj5KbKaDGD7dhjFIvM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:31+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" .
}