@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP577396.RAwjWKJQBML2qlKHYTUm77ocShGjbWtuu_jAkule_Xcao> .
@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:NP577396.RAwjWKJQBML2qlKHYTUm77ocShGjbWtuu_jAkule_Xcao130_head {
  this: np:hasAssertion dgn-np:NP577396.RAwjWKJQBML2qlKHYTUm77ocShGjbWtuu_jAkule_Xcao130_assertion;
    np:hasProvenance dgn-np:NP577396.RAwjWKJQBML2qlKHYTUm77ocShGjbWtuu_jAkule_Xcao130_provenance;
    np:hasPublicationInfo dgn-np:NP577396.RAwjWKJQBML2qlKHYTUm77ocShGjbWtuu_jAkule_Xcao130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP577396.RAwjWKJQBML2qlKHYTUm77ocShGjbWtuu_jAkule_Xcao130_assertion a np:Assertion .
  
  dgn-np:NP577396.RAwjWKJQBML2qlKHYTUm77ocShGjbWtuu_jAkule_Xcao130_provenance a np:Provenance .
  
  dgn-np:NP577396.RAwjWKJQBML2qlKHYTUm77ocShGjbWtuu_jAkule_Xcao130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP577396.RAwjWKJQBML2qlKHYTUm77ocShGjbWtuu_jAkule_Xcao130_assertion {
  miriam-gene:6103 a ncit:C16612 .
  
  lld:C0035309 a ncit:C7057 .
  
  dgn-gda:DGN52c0a57f2a20fcc076461e7889139d4f sio:SIO_000628 miriam-gene:6103, lld:C0035309;
    a sio:SIO_001121 .
}

dgn-np:NP577396.RAwjWKJQBML2qlKHYTUm77ocShGjbWtuu_jAkule_Xcao130_provenance {
  dgn-np:NP577396.RAwjWKJQBML2qlKHYTUm77ocShGjbWtuu_jAkule_Xcao130_assertion dcterms:description
      "[In this study, RPGRIP1, RANBP2, NPM1, PDE6D, NPHP5, and ABCA4 genes were selected on the basis of interaction with RPGR or RPGRIP1 or their implication in related retinal diseases, and were investigated as candidate genetic modifiers of XLPRA1.]. 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:17653054;
    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:NP577396.RAwjWKJQBML2qlKHYTUm77ocShGjbWtuu_jAkule_Xcao130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:48+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}