@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP703425.RACDvw9d0y87d6ffz8KOOUvXuxwOnJSYRMVId40Cy2zVE> .
@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:NP703425.RACDvw9d0y87d6ffz8KOOUvXuxwOnJSYRMVId40Cy2zVE130_head {
  this: np:hasAssertion dgn-np:NP703425.RACDvw9d0y87d6ffz8KOOUvXuxwOnJSYRMVId40Cy2zVE130_assertion;
    np:hasProvenance dgn-np:NP703425.RACDvw9d0y87d6ffz8KOOUvXuxwOnJSYRMVId40Cy2zVE130_provenance;
    np:hasPublicationInfo dgn-np:NP703425.RACDvw9d0y87d6ffz8KOOUvXuxwOnJSYRMVId40Cy2zVE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP703425.RACDvw9d0y87d6ffz8KOOUvXuxwOnJSYRMVId40Cy2zVE130_assertion a np:Assertion .
  
  dgn-np:NP703425.RACDvw9d0y87d6ffz8KOOUvXuxwOnJSYRMVId40Cy2zVE130_provenance a np:Provenance .
  
  dgn-np:NP703425.RACDvw9d0y87d6ffz8KOOUvXuxwOnJSYRMVId40Cy2zVE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP703425.RACDvw9d0y87d6ffz8KOOUvXuxwOnJSYRMVId40Cy2zVE130_assertion {
  miriam-gene:5158 a ncit:C16612 .
  
  lld:C0035334 a ncit:C7057 .
  
  dgn-gda:DGN24969da551dfbd973b87ee0b737eb597 sio:SIO_000628 miriam-gene:5158, lld:C0035334;
    a sio:SIO_001121 .
}

dgn-np:NP703425.RACDvw9d0y87d6ffz8KOOUvXuxwOnJSYRMVId40Cy2zVE130_provenance {
  dgn-np:NP703425.RACDvw9d0y87d6ffz8KOOUvXuxwOnJSYRMVId40Cy2zVE130_assertion dcterms:description
      "[Mutations in PDE6A and the PDE6B genes lead to autosomal recessive (ar) forms of retinitis pigmentosa (RP) in human and to the homologous disease in dogs, designated generalised progressive retinal atrophy (gPRA).]. 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:10782214;
    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:NP703425.RACDvw9d0y87d6ffz8KOOUvXuxwOnJSYRMVId40Cy2zVE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:07+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" .
}