@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP231704.RAr2Bt9v3FxJnL4GY9ney7nNVMgtu1s3nxskPq7D6VZaI> .
@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:NP231704.RAr2Bt9v3FxJnL4GY9ney7nNVMgtu1s3nxskPq7D6VZaI130_head {
  this: np:hasAssertion dgn-np:NP231704.RAr2Bt9v3FxJnL4GY9ney7nNVMgtu1s3nxskPq7D6VZaI130_assertion;
    np:hasProvenance dgn-np:NP231704.RAr2Bt9v3FxJnL4GY9ney7nNVMgtu1s3nxskPq7D6VZaI130_provenance;
    np:hasPublicationInfo dgn-np:NP231704.RAr2Bt9v3FxJnL4GY9ney7nNVMgtu1s3nxskPq7D6VZaI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP231704.RAr2Bt9v3FxJnL4GY9ney7nNVMgtu1s3nxskPq7D6VZaI130_assertion a np:Assertion .
  
  dgn-np:NP231704.RAr2Bt9v3FxJnL4GY9ney7nNVMgtu1s3nxskPq7D6VZaI130_provenance a np:Provenance .
  
  dgn-np:NP231704.RAr2Bt9v3FxJnL4GY9ney7nNVMgtu1s3nxskPq7D6VZaI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP231704.RAr2Bt9v3FxJnL4GY9ney7nNVMgtu1s3nxskPq7D6VZaI130_assertion {
  miriam-gene:6652 a ncit:C16612 .
  
  lld:C0011847 a ncit:C7057 .
  
  dgn-gda:DGN0512baeec1ab6da77297299084ae0b7e sio:SIO_000628 miriam-gene:6652, lld:C0011847;
    a sio:SIO_001121 .
}

dgn-np:NP231704.RAr2Bt9v3FxJnL4GY9ney7nNVMgtu1s3nxskPq7D6VZaI130_provenance {
  dgn-np:NP231704.RAr2Bt9v3FxJnL4GY9ney7nNVMgtu1s3nxskPq7D6VZaI130_assertion dcterms:description
      "[These results do not define a clear cataract-SORD deficiency etiopathogenic relationship, nevertheless, they strongly suggest activity polymorphism in human red cell SORD, which would be highly relevant not only to the study of cataracts but of other major complications in diabetes.]. 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:7152518;
    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:NP231704.RAr2Bt9v3FxJnL4GY9ney7nNVMgtu1s3nxskPq7D6VZaI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:10+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" .
}