@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP167034.RAS8nW6fD5JLqPoJWcckIyDvmRH_9HmP0CtKRkmqeemNs> .
@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:NP167034.RAS8nW6fD5JLqPoJWcckIyDvmRH_9HmP0CtKRkmqeemNs130_head {
  this: np:hasAssertion dgn-np:NP167034.RAS8nW6fD5JLqPoJWcckIyDvmRH_9HmP0CtKRkmqeemNs130_assertion;
    np:hasProvenance dgn-np:NP167034.RAS8nW6fD5JLqPoJWcckIyDvmRH_9HmP0CtKRkmqeemNs130_provenance;
    np:hasPublicationInfo dgn-np:NP167034.RAS8nW6fD5JLqPoJWcckIyDvmRH_9HmP0CtKRkmqeemNs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP167034.RAS8nW6fD5JLqPoJWcckIyDvmRH_9HmP0CtKRkmqeemNs130_assertion a np:Assertion .
  
  dgn-np:NP167034.RAS8nW6fD5JLqPoJWcckIyDvmRH_9HmP0CtKRkmqeemNs130_provenance a np:Provenance .
  
  dgn-np:NP167034.RAS8nW6fD5JLqPoJWcckIyDvmRH_9HmP0CtKRkmqeemNs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP167034.RAS8nW6fD5JLqPoJWcckIyDvmRH_9HmP0CtKRkmqeemNs130_assertion {
  miriam-gene:2078 a ncit:C16612 .
  
  lld:C0339525 a ncit:C7057 .
  
  dgn-gda:DGN3a0577ff6f1c062213066850f188dc77 sio:SIO_000628 miriam-gene:2078, lld:C0339525;
    a sio:SIO_001121 .
}

dgn-np:NP167034.RAS8nW6fD5JLqPoJWcckIyDvmRH_9HmP0CtKRkmqeemNs130_provenance {
  dgn-np:NP167034.RAS8nW6fD5JLqPoJWcckIyDvmRH_9HmP0CtKRkmqeemNs130_assertion dcterms:description
      "[These patients (mean age, 36.6 years) had, on average, significantly better visual acuity and larger ERG amplitudes than 131 unrelated patients (mean age, 32.1 years) with autosomal dominant retinitis pigmentosa without this mutation.]. 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:2095030;
    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:NP167034.RAS8nW6fD5JLqPoJWcckIyDvmRH_9HmP0CtKRkmqeemNs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:30+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" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}