@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP244386.RAOiQPPFpvHCJZevks2pjIjvnthXeOXJ_c40FrPLqYayg> .
@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:NP244386.RAOiQPPFpvHCJZevks2pjIjvnthXeOXJ_c40FrPLqYayg130_head {
  this: np:hasAssertion dgn-np:NP244386.RAOiQPPFpvHCJZevks2pjIjvnthXeOXJ_c40FrPLqYayg130_assertion;
    np:hasProvenance dgn-np:NP244386.RAOiQPPFpvHCJZevks2pjIjvnthXeOXJ_c40FrPLqYayg130_provenance;
    np:hasPublicationInfo dgn-np:NP244386.RAOiQPPFpvHCJZevks2pjIjvnthXeOXJ_c40FrPLqYayg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP244386.RAOiQPPFpvHCJZevks2pjIjvnthXeOXJ_c40FrPLqYayg130_assertion a np:Assertion .
  
  dgn-np:NP244386.RAOiQPPFpvHCJZevks2pjIjvnthXeOXJ_c40FrPLqYayg130_provenance a np:Provenance .
  
  dgn-np:NP244386.RAOiQPPFpvHCJZevks2pjIjvnthXeOXJ_c40FrPLqYayg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP244386.RAOiQPPFpvHCJZevks2pjIjvnthXeOXJ_c40FrPLqYayg130_assertion {
  miriam-gene:26121 a ncit:C16612 .
  
  lld:C0035334 a ncit:C7057 .
  
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    a sio:SIO_001121 .
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dgn-np:NP244386.RAOiQPPFpvHCJZevks2pjIjvnthXeOXJ_c40FrPLqYayg130_provenance {
  dgn-np:NP244386.RAOiQPPFpvHCJZevks2pjIjvnthXeOXJ_c40FrPLqYayg130_assertion dcterms:description
      "[These findings significantly impact our understanding of the molecular mechanisms underlying RP and suggest that the insufficiency of the functional hPrp31 protein combined with the potential cytotoxicity associated with the expression the AD29 mutant are at least partially causative of the RP phenotype.]. 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:19293337;
    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:NP244386.RAOiQPPFpvHCJZevks2pjIjvnthXeOXJ_c40FrPLqYayg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:16+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:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}