@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP599158.RAd29HDXewbgzc1lFUUis0K4HiqRydTYqxdEp17gZlhqM> .
@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:NP599158.RAd29HDXewbgzc1lFUUis0K4HiqRydTYqxdEp17gZlhqM130_head {
  this: np:hasAssertion dgn-np:NP599158.RAd29HDXewbgzc1lFUUis0K4HiqRydTYqxdEp17gZlhqM130_assertion ;
    np:hasProvenance dgn-np:NP599158.RAd29HDXewbgzc1lFUUis0K4HiqRydTYqxdEp17gZlhqM130_provenance ;
    np:hasPublicationInfo dgn-np:NP599158.RAd29HDXewbgzc1lFUUis0K4HiqRydTYqxdEp17gZlhqM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP599158.RAd29HDXewbgzc1lFUUis0K4HiqRydTYqxdEp17gZlhqM130_assertion a np:Assertion .
  dgn-np:NP599158.RAd29HDXewbgzc1lFUUis0K4HiqRydTYqxdEp17gZlhqM130_provenance a np:Provenance .
  dgn-np:NP599158.RAd29HDXewbgzc1lFUUis0K4HiqRydTYqxdEp17gZlhqM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP599158.RAd29HDXewbgzc1lFUUis0K4HiqRydTYqxdEp17gZlhqM130_assertion {
  miriam-gene:4901 a ncit:C16612 .
  lld:C0034951 a ncit:C7057 .
  dgn-gda:DGN8a284169a43d970626cf84ba2a675ef6 sio:SIO_000628 miriam-gene:4901 , lld:C0034951 ;
    a sio:SIO_001122 .
}
dgn-np:NP599158.RAd29HDXewbgzc1lFUUis0K4HiqRydTYqxdEp17gZlhqM130_provenance {
  dgn-np:NP599158.RAd29HDXewbgzc1lFUUis0K4HiqRydTYqxdEp17gZlhqM130_assertion dcterms:description "[The dark-adaptation thresholds, equivalent visual field diameters, and electroretinogram amplitudes (all corrected for age and refractive error) indicated that the disease caused by the NRL mutations was more severe than that caused by the dominant rhodopsin mutation Pro23His and was similar in severity to that produced by the rhodopsin mutation Pro347Leu.]. 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:11879142 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP599158.RAd29HDXewbgzc1lFUUis0K4HiqRydTYqxdEp17gZlhqM130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:38+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:disgenetv3.0rdf ;
    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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}