@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP671637.RAS271P2qMPkS2aUakWwAuZEcFkPEOfh8a8kDRnrGjc4M> .
@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:NP671637.RAS271P2qMPkS2aUakWwAuZEcFkPEOfh8a8kDRnrGjc4M130_head {
  this: np:hasAssertion dgn-np:NP671637.RAS271P2qMPkS2aUakWwAuZEcFkPEOfh8a8kDRnrGjc4M130_assertion;
    np:hasProvenance dgn-np:NP671637.RAS271P2qMPkS2aUakWwAuZEcFkPEOfh8a8kDRnrGjc4M130_provenance;
    np:hasPublicationInfo dgn-np:NP671637.RAS271P2qMPkS2aUakWwAuZEcFkPEOfh8a8kDRnrGjc4M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP671637.RAS271P2qMPkS2aUakWwAuZEcFkPEOfh8a8kDRnrGjc4M130_assertion a np:Assertion .
  
  dgn-np:NP671637.RAS271P2qMPkS2aUakWwAuZEcFkPEOfh8a8kDRnrGjc4M130_provenance a np:Provenance .
  
  dgn-np:NP671637.RAS271P2qMPkS2aUakWwAuZEcFkPEOfh8a8kDRnrGjc4M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP671637.RAS271P2qMPkS2aUakWwAuZEcFkPEOfh8a8kDRnrGjc4M130_assertion {
  miriam-gene:5995 a ncit:C16612 .
  
  lld:C0035334 a ncit:C7057 .
  
  dgn-gda:DGNf8b41f9f1aeee8d3bfd7942ca4a22b3b sio:SIO_000628 miriam-gene:5995, lld:C0035334;
    a sio:SIO_001121 .
}

dgn-np:NP671637.RAS271P2qMPkS2aUakWwAuZEcFkPEOfh8a8kDRnrGjc4M130_provenance {
  dgn-np:NP671637.RAS271P2qMPkS2aUakWwAuZEcFkPEOfh8a8kDRnrGjc4M130_assertion dcterms:description
      "[We used denaturing high performance liquid chromatography (D-HPLC) and direct sequencing to screen 216 patients (134 with autosomal recessive or sporadic retinitis pigmentosa (RP) and 82 with other retinal dystrophies) for RBP1 and RBP3, and 331 patients for RGR (79 cases with autosomal dominant RP and 36 RP cases with undetermined inheritance were added to the 216 previous patients).]. 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:21067480;
    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:NP671637.RAS271P2qMPkS2aUakWwAuZEcFkPEOfh8a8kDRnrGjc4M130_publicationInfo {
  this: dcterms:created "2015-08-25T14:44:24+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" .
}