@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP255834.RA5DfNXkCYcWS7Bs9cQ6e6j9SI8aDBPYHxorKMiKI4cV0> .
@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:NP255834.RA5DfNXkCYcWS7Bs9cQ6e6j9SI8aDBPYHxorKMiKI4cV0130_head {
  this: np:hasAssertion dgn-np:NP255834.RA5DfNXkCYcWS7Bs9cQ6e6j9SI8aDBPYHxorKMiKI4cV0130_assertion;
    np:hasProvenance dgn-np:NP255834.RA5DfNXkCYcWS7Bs9cQ6e6j9SI8aDBPYHxorKMiKI4cV0130_provenance;
    np:hasPublicationInfo dgn-np:NP255834.RA5DfNXkCYcWS7Bs9cQ6e6j9SI8aDBPYHxorKMiKI4cV0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP255834.RA5DfNXkCYcWS7Bs9cQ6e6j9SI8aDBPYHxorKMiKI4cV0130_assertion a np:Assertion .
  
  dgn-np:NP255834.RA5DfNXkCYcWS7Bs9cQ6e6j9SI8aDBPYHxorKMiKI4cV0130_provenance a np:Provenance .
  
  dgn-np:NP255834.RA5DfNXkCYcWS7Bs9cQ6e6j9SI8aDBPYHxorKMiKI4cV0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP255834.RA5DfNXkCYcWS7Bs9cQ6e6j9SI8aDBPYHxorKMiKI4cV0130_assertion {
  miriam-gene:23746 a ncit:C16612 .
  
  lld:C0521683 a ncit:C7057 .
  
  dgn-gda:DGN87a0df969445fd0e9d8bf2220f613a50 sio:SIO_000628 miriam-gene:23746, lld:C0521683;
    a sio:SIO_001121 .
}

dgn-np:NP255834.RA5DfNXkCYcWS7Bs9cQ6e6j9SI8aDBPYHxorKMiKI4cV0130_provenance {
  dgn-np:NP255834.RA5DfNXkCYcWS7Bs9cQ6e6j9SI8aDBPYHxorKMiKI4cV0130_assertion dcterms:description
      "[Drusenlike deposits were more selectively observed in patients with mutations in the AIPL1, CRB1, RPE65, and RPGRIP1 genes, whereas focal regions of peripheral chorioretinal atrophy were observed only in patients with AIPL1 or RPE65 variations.]. 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:16205573;
    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:NP255834.RA5DfNXkCYcWS7Bs9cQ6e6j9SI8aDBPYHxorKMiKI4cV0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:23+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" .
}