@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP312509.RAG-h_CPRLjTGSNqSiAd-cOfPNI7hT1y28PD17vTm0A-0> .
@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:NP312509.RAG-h_CPRLjTGSNqSiAd-cOfPNI7hT1y28PD17vTm0A-0130_head {
  this: np:hasAssertion dgn-np:NP312509.RAG-h_CPRLjTGSNqSiAd-cOfPNI7hT1y28PD17vTm0A-0130_assertion;
    np:hasProvenance dgn-np:NP312509.RAG-h_CPRLjTGSNqSiAd-cOfPNI7hT1y28PD17vTm0A-0130_provenance;
    np:hasPublicationInfo dgn-np:NP312509.RAG-h_CPRLjTGSNqSiAd-cOfPNI7hT1y28PD17vTm0A-0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP312509.RAG-h_CPRLjTGSNqSiAd-cOfPNI7hT1y28PD17vTm0A-0130_assertion a np:Assertion .
  
  dgn-np:NP312509.RAG-h_CPRLjTGSNqSiAd-cOfPNI7hT1y28PD17vTm0A-0130_provenance a np:Provenance .
  
  dgn-np:NP312509.RAG-h_CPRLjTGSNqSiAd-cOfPNI7hT1y28PD17vTm0A-0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP312509.RAG-h_CPRLjTGSNqSiAd-cOfPNI7hT1y28PD17vTm0A-0130_assertion {
  miriam-gene:231 a ncit:C16612 .
  
  lld:C0442874 a ncit:C7057 .
  
  dgn-gda:DGN539a07d85c9ce85e94dc4f83ddddda5a sio:SIO_000628 miriam-gene:231, lld:C0442874;
    a sio:SIO_001121 .
}

dgn-np:NP312509.RAG-h_CPRLjTGSNqSiAd-cOfPNI7hT1y28PD17vTm0A-0130_provenance {
  dgn-np:NP312509.RAG-h_CPRLjTGSNqSiAd-cOfPNI7hT1y28PD17vTm0A-0130_assertion dcterms:description
      "[Recently an (A-C)n dinucleotide repeat polymorphic marker in the 5'-region of the ALR2 gene encoding aldose reductase was found to be associated with diabetic retinopathy in the Chinese population in Hong Kong, and with nephropathy and neuropathy in the British Caucasian population.]. 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:10510950;
    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:NP312509.RAG-h_CPRLjTGSNqSiAd-cOfPNI7hT1y28PD17vTm0A-0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:59+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" .
}