@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP948162.RAjcp5-jY8w64LvzLUotOXPGFDzK4uIJDepRlouyTnSDI> .
@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:NP948162.RAjcp5-jY8w64LvzLUotOXPGFDzK4uIJDepRlouyTnSDI130_head {
  this: np:hasAssertion dgn-np:NP948162.RAjcp5-jY8w64LvzLUotOXPGFDzK4uIJDepRlouyTnSDI130_assertion ;
    np:hasProvenance dgn-np:NP948162.RAjcp5-jY8w64LvzLUotOXPGFDzK4uIJDepRlouyTnSDI130_provenance ;
    np:hasPublicationInfo dgn-np:NP948162.RAjcp5-jY8w64LvzLUotOXPGFDzK4uIJDepRlouyTnSDI130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP948162.RAjcp5-jY8w64LvzLUotOXPGFDzK4uIJDepRlouyTnSDI130_provenance a np:Provenance .
  dgn-np:NP948162.RAjcp5-jY8w64LvzLUotOXPGFDzK4uIJDepRlouyTnSDI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP948162.RAjcp5-jY8w64LvzLUotOXPGFDzK4uIJDepRlouyTnSDI130_assertion {
  miriam-gene:80184 a ncit:C16612 .
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}
dgn-np:NP948162.RAjcp5-jY8w64LvzLUotOXPGFDzK4uIJDepRlouyTnSDI130_provenance {
  dgn-np:NP948162.RAjcp5-jY8w64LvzLUotOXPGFDzK4uIJDepRlouyTnSDI130_assertion dcterms:description "[Our findings add to the increasing body of evidence that ciliopathies can cause a broad spectrum of disease phenotypes, and pleiotropic effects of CEP290 mutations range from single organ involvement with isolated Leber congenital amaurosis to Joubert syndrome and lethal early embryonic multisystemic malformations in Meckel-Gruber syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    prov:wasDerivedFrom dgn-void:befree-20150227 ;
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}
dgn-np:NP948162.RAjcp5-jY8w64LvzLUotOXPGFDzK4uIJDepRlouyTnSDI130_publicationInfo {
  this: dcterms:created "2015-08-25T14:47:19+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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}