@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP402838.RAs6JIs-aFCOBOrerZms7yBxiOAAeUPzPwxyHovm6Xbdw> .
@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:NP402838.RAs6JIs-aFCOBOrerZms7yBxiOAAeUPzPwxyHovm6Xbdw130_head {
  this: np:hasAssertion dgn-np:NP402838.RAs6JIs-aFCOBOrerZms7yBxiOAAeUPzPwxyHovm6Xbdw130_assertion ;
    np:hasProvenance dgn-np:NP402838.RAs6JIs-aFCOBOrerZms7yBxiOAAeUPzPwxyHovm6Xbdw130_provenance ;
    np:hasPublicationInfo dgn-np:NP402838.RAs6JIs-aFCOBOrerZms7yBxiOAAeUPzPwxyHovm6Xbdw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP402838.RAs6JIs-aFCOBOrerZms7yBxiOAAeUPzPwxyHovm6Xbdw130_assertion a np:Assertion .
  dgn-np:NP402838.RAs6JIs-aFCOBOrerZms7yBxiOAAeUPzPwxyHovm6Xbdw130_provenance a np:Provenance .
  dgn-np:NP402838.RAs6JIs-aFCOBOrerZms7yBxiOAAeUPzPwxyHovm6Xbdw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP402838.RAs6JIs-aFCOBOrerZms7yBxiOAAeUPzPwxyHovm6Xbdw130_assertion {
  miriam-gene:3757 a ncit:C16612 .
  lld:C0008525 a ncit:C7057 .
  dgn-gda:DGN2bf9304bfa4d5acf90b2561702d446d5 sio:SIO_000628 miriam-gene:3757 , lld:C0008525 ;
    a sio:SIO_001121 .
}
dgn-np:NP402838.RAs6JIs-aFCOBOrerZms7yBxiOAAeUPzPwxyHovm6Xbdw130_provenance {
  dgn-np:NP402838.RAs6JIs-aFCOBOrerZms7yBxiOAAeUPzPwxyHovm6Xbdw130_assertion dcterms:description "[The carriers of XLRP who had evidence of photoreceptor cell dysfunction (as determined by visual field loss and reduced ERG amplitudes) had increased levels of intraocular straylight, whereas the carriers of CHM, who showed fundus abnormalities alone, in the absence of demonstrable photoreceptor cell dysfunction, had normal or minimally elevated levels.]. 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:11772598 ;
    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:NP402838.RAs6JIs-aFCOBOrerZms7yBxiOAAeUPzPwxyHovm6Xbdw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:00+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> , <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 "v2.1.0.0" .
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}