@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP441897.RAq2CPR5MFkwt2_DnDlZ1Z2AJh2kq8tdYdoUOY1PrRsPQ> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP441897.RAq2CPR5MFkwt2_DnDlZ1Z2AJh2kq8tdYdoUOY1PrRsPQ130_head {
  this: np:hasAssertion dgn-np:NP441897.RAq2CPR5MFkwt2_DnDlZ1Z2AJh2kq8tdYdoUOY1PrRsPQ130_assertion;
    np:hasProvenance dgn-np:NP441897.RAq2CPR5MFkwt2_DnDlZ1Z2AJh2kq8tdYdoUOY1PrRsPQ130_provenance;
    np:hasPublicationInfo dgn-np:NP441897.RAq2CPR5MFkwt2_DnDlZ1Z2AJh2kq8tdYdoUOY1PrRsPQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP441897.RAq2CPR5MFkwt2_DnDlZ1Z2AJh2kq8tdYdoUOY1PrRsPQ130_assertion a np:Assertion .
  
  dgn-np:NP441897.RAq2CPR5MFkwt2_DnDlZ1Z2AJh2kq8tdYdoUOY1PrRsPQ130_provenance a np:Provenance .
  
  dgn-np:NP441897.RAq2CPR5MFkwt2_DnDlZ1Z2AJh2kq8tdYdoUOY1PrRsPQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP441897.RAq2CPR5MFkwt2_DnDlZ1Z2AJh2kq8tdYdoUOY1PrRsPQ130_assertion {
  miriam-gene:2978 a ncit:C16612 .
  
  lld:C0242383 a ncit:C7057 .
  
  dgn-gda:DGNf879485f5ef27d7f35d9134192cad14d sio:SIO_000628 miriam-gene:2978, lld:C0242383;
    a sio:SIO_001121 .
}

dgn-np:NP441897.RAq2CPR5MFkwt2_DnDlZ1Z2AJh2kq8tdYdoUOY1PrRsPQ130_provenance {
  dgn-np:NP441897.RAq2CPR5MFkwt2_DnDlZ1Z2AJh2kq8tdYdoUOY1PrRsPQ130_assertion dcterms:description
      "[The patients analyzed included 52 with autosomal dominant retinitis pigmentosa, 36 with autosomal recessive retinitis pigmentosa, 3 with simplex retinitis pigmentosa, 12 with cone-rod dystrophy, 5 with rod-cone dystrophy, 3 with vitelliform macular dystrophy (Best's disease), 4 with macular dystrophy, 2 with cone dystrophy, 2 with fundus flavimaculatus, 2 with fundus albipunctatus, and 12 with retinitis pigmentosa with macular degeneration as well as 40 unrelated normal persons.]. 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:9690896;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP441897.RAq2CPR5MFkwt2_DnDlZ1Z2AJh2kq8tdYdoUOY1PrRsPQ130_publicationInfo {
  this: dcterms:created "2015-08-25T14:41:58+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}