@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP217848.RABVHU1PheENsgqFSq82ejOiwDY9ulQXaI1ymoprtpuF4> .
@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:NP217848.RABVHU1PheENsgqFSq82ejOiwDY9ulQXaI1ymoprtpuF4130_head {
  this: np:hasAssertion dgn-np:NP217848.RABVHU1PheENsgqFSq82ejOiwDY9ulQXaI1ymoprtpuF4130_assertion;
    np:hasProvenance dgn-np:NP217848.RABVHU1PheENsgqFSq82ejOiwDY9ulQXaI1ymoprtpuF4130_provenance;
    np:hasPublicationInfo dgn-np:NP217848.RABVHU1PheENsgqFSq82ejOiwDY9ulQXaI1ymoprtpuF4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP217848.RABVHU1PheENsgqFSq82ejOiwDY9ulQXaI1ymoprtpuF4130_assertion a np:Assertion .
  
  dgn-np:NP217848.RABVHU1PheENsgqFSq82ejOiwDY9ulQXaI1ymoprtpuF4130_provenance a np:Provenance .
  
  dgn-np:NP217848.RABVHU1PheENsgqFSq82ejOiwDY9ulQXaI1ymoprtpuF4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP217848.RABVHU1PheENsgqFSq82ejOiwDY9ulQXaI1ymoprtpuF4130_assertion {
  miriam-gene:5961 a ncit:C16612 .
  
  lld:C1320640 a ncit:C7057 .
  
  dgn-gda:DGNe7ed99bd02a5bd90cf8ecbc950a27e72 sio:SIO_000628 miriam-gene:5961, lld:C1320640;
    a sio:SIO_001121 .
}

dgn-np:NP217848.RABVHU1PheENsgqFSq82ejOiwDY9ulQXaI1ymoprtpuF4130_provenance {
  dgn-np:NP217848.RABVHU1PheENsgqFSq82ejOiwDY9ulQXaI1ymoprtpuF4130_assertion dcterms:description
      "[The RDS gene has been implicated in the mouse phenotype retinal degeneration slow, and mutations in the human homologue are now known to be associated with both central and peripheral retinal degenerations.]. 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:8956033;
    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:NP217848.RABVHU1PheENsgqFSq82ejOiwDY9ulQXaI1ymoprtpuF4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:01+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" .
}