@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP628522.RAZ4zQ-eObPe6riB-M48MMzGd7DtphSFljqgXc3313lAg> .
@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:NP628522.RAZ4zQ-eObPe6riB-M48MMzGd7DtphSFljqgXc3313lAg130_head {
  this: np:hasAssertion dgn-np:NP628522.RAZ4zQ-eObPe6riB-M48MMzGd7DtphSFljqgXc3313lAg130_assertion;
    np:hasProvenance dgn-np:NP628522.RAZ4zQ-eObPe6riB-M48MMzGd7DtphSFljqgXc3313lAg130_provenance;
    np:hasPublicationInfo dgn-np:NP628522.RAZ4zQ-eObPe6riB-M48MMzGd7DtphSFljqgXc3313lAg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP628522.RAZ4zQ-eObPe6riB-M48MMzGd7DtphSFljqgXc3313lAg130_assertion a np:Assertion .
  
  dgn-np:NP628522.RAZ4zQ-eObPe6riB-M48MMzGd7DtphSFljqgXc3313lAg130_provenance a np:Provenance .
  
  dgn-np:NP628522.RAZ4zQ-eObPe6riB-M48MMzGd7DtphSFljqgXc3313lAg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP628522.RAZ4zQ-eObPe6riB-M48MMzGd7DtphSFljqgXc3313lAg130_assertion {
  miriam-gene:89866 a ncit:C16612 .
  
  lld:C0035304 a ncit:C7057 .
  
  dgn-gda:DGNd1cb62ae7f9aeef7817ee3fad5f61a5c sio:SIO_000628 miriam-gene:89866, lld:C0035304;
    a sio:SIO_001121 .
}

dgn-np:NP628522.RAZ4zQ-eObPe6riB-M48MMzGd7DtphSFljqgXc3313lAg130_provenance {
  dgn-np:NP628522.RAZ4zQ-eObPe6riB-M48MMzGd7DtphSFljqgXc3313lAg130_assertion dcterms:description
      "[RGPR was the first gene found to be mutated in XLRP, the subtype of RP displaying the most severe form of retinal degeneration with partial or complete blindness in the third or fourth decade of life.]. 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:12402343;
    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:NP628522.RAZ4zQ-eObPe6riB-M48MMzGd7DtphSFljqgXc3313lAg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:19+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" .
}