@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP240371.RATHVZJNRRFffFCSkFDQEyHqbAbL2yo5QW0gV8o7G2RLw> .
@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:NP240371.RATHVZJNRRFffFCSkFDQEyHqbAbL2yo5QW0gV8o7G2RLw130_head {
  this: np:hasAssertion dgn-np:NP240371.RATHVZJNRRFffFCSkFDQEyHqbAbL2yo5QW0gV8o7G2RLw130_assertion;
    np:hasProvenance dgn-np:NP240371.RATHVZJNRRFffFCSkFDQEyHqbAbL2yo5QW0gV8o7G2RLw130_provenance;
    np:hasPublicationInfo dgn-np:NP240371.RATHVZJNRRFffFCSkFDQEyHqbAbL2yo5QW0gV8o7G2RLw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP240371.RATHVZJNRRFffFCSkFDQEyHqbAbL2yo5QW0gV8o7G2RLw130_assertion a np:Assertion .
  
  dgn-np:NP240371.RATHVZJNRRFffFCSkFDQEyHqbAbL2yo5QW0gV8o7G2RLw130_provenance a np:Provenance .
  
  dgn-np:NP240371.RATHVZJNRRFffFCSkFDQEyHqbAbL2yo5QW0gV8o7G2RLw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP240371.RATHVZJNRRFffFCSkFDQEyHqbAbL2yo5QW0gV8o7G2RLw130_assertion {
  miriam-gene:26121 a ncit:C16612 .
  
  lld:C0339525 a ncit:C7057 .
  
  dgn-gda:DGN8bdf9be425a2d1c626148bf2389a057d sio:SIO_000628 miriam-gene:26121, lld:C0339525;
    a sio:SIO_001121 .
}

dgn-np:NP240371.RATHVZJNRRFffFCSkFDQEyHqbAbL2yo5QW0gV8o7G2RLw130_provenance {
  dgn-np:NP240371.RATHVZJNRRFffFCSkFDQEyHqbAbL2yo5QW0gV8o7G2RLw130_assertion dcterms:description
      "[To identify the mutations in the pre-mRNA processing factor 31 homolog (PRPF31) gene in Chinese families with autosomal dominant retinitis pigmentosa (adRP) and to characterize the clinical features of those patients who were found to have mutations in the PRPF31 gene.]. 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:23288994;
    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:NP240371.RATHVZJNRRFffFCSkFDQEyHqbAbL2yo5QW0gV8o7G2RLw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:14+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" .
}