@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP217981.RAAb1Lep2Y_uepHGFtD7iNZZQjSoDk9GvlkrUvcMVXKwc> .
@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:NP217981.RAAb1Lep2Y_uepHGFtD7iNZZQjSoDk9GvlkrUvcMVXKwc130_head {
  this: np:hasAssertion dgn-np:NP217981.RAAb1Lep2Y_uepHGFtD7iNZZQjSoDk9GvlkrUvcMVXKwc130_assertion;
    np:hasProvenance dgn-np:NP217981.RAAb1Lep2Y_uepHGFtD7iNZZQjSoDk9GvlkrUvcMVXKwc130_provenance;
    np:hasPublicationInfo dgn-np:NP217981.RAAb1Lep2Y_uepHGFtD7iNZZQjSoDk9GvlkrUvcMVXKwc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP217981.RAAb1Lep2Y_uepHGFtD7iNZZQjSoDk9GvlkrUvcMVXKwc130_assertion a np:Assertion .
  
  dgn-np:NP217981.RAAb1Lep2Y_uepHGFtD7iNZZQjSoDk9GvlkrUvcMVXKwc130_provenance a np:Provenance .
  
  dgn-np:NP217981.RAAb1Lep2Y_uepHGFtD7iNZZQjSoDk9GvlkrUvcMVXKwc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP217981.RAAb1Lep2Y_uepHGFtD7iNZZQjSoDk9GvlkrUvcMVXKwc130_assertion {
  miriam-gene:3630 a ncit:C16612 .
  
  lld:C1998028 a ncit:C7057 .
  
  dgn-gda:DGN00e7d2910a4a829feed83eefba04d105 sio:SIO_000628 miriam-gene:3630, lld:C1998028;
    a sio:SIO_001121 .
}

dgn-np:NP217981.RAAb1Lep2Y_uepHGFtD7iNZZQjSoDk9GvlkrUvcMVXKwc130_provenance {
  dgn-np:NP217981.RAAb1Lep2Y_uepHGFtD7iNZZQjSoDk9GvlkrUvcMVXKwc130_assertion dcterms:description
      "[In this work we assess the therapeutic potential of proinsulin on photoreceptor degeneration, synaptic connectivity, and functional activity of the retina in the transgenic P23H rat, an animal model of autosomal dominant retinitis pigmentosa (RP).]. 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:23017108;
    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:NP217981.RAAb1Lep2Y_uepHGFtD7iNZZQjSoDk9GvlkrUvcMVXKwc130_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" .
}