@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP863050.RAjyNwL53f7g-HPLWcMSZwsUaiqaMu9WVcToc9hG-bkvE> .
@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:NP863050.RAjyNwL53f7g-HPLWcMSZwsUaiqaMu9WVcToc9hG-bkvE130_head {
  this: np:hasAssertion dgn-np:NP863050.RAjyNwL53f7g-HPLWcMSZwsUaiqaMu9WVcToc9hG-bkvE130_assertion;
    np:hasProvenance dgn-np:NP863050.RAjyNwL53f7g-HPLWcMSZwsUaiqaMu9WVcToc9hG-bkvE130_provenance;
    np:hasPublicationInfo dgn-np:NP863050.RAjyNwL53f7g-HPLWcMSZwsUaiqaMu9WVcToc9hG-bkvE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP863050.RAjyNwL53f7g-HPLWcMSZwsUaiqaMu9WVcToc9hG-bkvE130_assertion a np:Assertion .
  
  dgn-np:NP863050.RAjyNwL53f7g-HPLWcMSZwsUaiqaMu9WVcToc9hG-bkvE130_provenance a np:Provenance .
  
  dgn-np:NP863050.RAjyNwL53f7g-HPLWcMSZwsUaiqaMu9WVcToc9hG-bkvE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP863050.RAjyNwL53f7g-HPLWcMSZwsUaiqaMu9WVcToc9hG-bkvE130_assertion {
  miriam-gene:6103 a ncit:C16612 .
  
  lld:C0524851 a ncit:C7057 .
  
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    a sio:SIO_001121 .
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dgn-np:NP863050.RAjyNwL53f7g-HPLWcMSZwsUaiqaMu9WVcToc9hG-bkvE130_provenance {
  dgn-np:NP863050.RAjyNwL53f7g-HPLWcMSZwsUaiqaMu9WVcToc9hG-bkvE130_assertion dcterms:description
      "[This review highlights the progress devoted to understand the pathogenesis associated with XlRP3 and allied disorders and, concepts, trends and discrepancies emerging as molecular, subcellular and physiological processes linked to RPGR and RPGRIP1-protein network begin to be elucidated, and that may serve as a paradigm for other biological processes and neurodegenerative diseases.]. 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-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:NP863050.RAjyNwL53f7g-HPLWcMSZwsUaiqaMu9WVcToc9hG-bkvE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:47+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" .
}