@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP376932.RAFg3R7C5nc2agNfzhWIWA9Z3R3LN4i50GaFbCCNbPRF0> .
@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:NP376932.RAFg3R7C5nc2agNfzhWIWA9Z3R3LN4i50GaFbCCNbPRF0130_head {
  this: np:hasAssertion dgn-np:NP376932.RAFg3R7C5nc2agNfzhWIWA9Z3R3LN4i50GaFbCCNbPRF0130_assertion;
    np:hasProvenance dgn-np:NP376932.RAFg3R7C5nc2agNfzhWIWA9Z3R3LN4i50GaFbCCNbPRF0130_provenance;
    np:hasPublicationInfo dgn-np:NP376932.RAFg3R7C5nc2agNfzhWIWA9Z3R3LN4i50GaFbCCNbPRF0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP376932.RAFg3R7C5nc2agNfzhWIWA9Z3R3LN4i50GaFbCCNbPRF0130_assertion a np:Assertion .
  
  dgn-np:NP376932.RAFg3R7C5nc2agNfzhWIWA9Z3R3LN4i50GaFbCCNbPRF0130_provenance a np:Provenance .
  
  dgn-np:NP376932.RAFg3R7C5nc2agNfzhWIWA9Z3R3LN4i50GaFbCCNbPRF0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP376932.RAFg3R7C5nc2agNfzhWIWA9Z3R3LN4i50GaFbCCNbPRF0130_assertion {
  miriam-gene:6652 a ncit:C16612 .
  
  lld:C0521707 a ncit:C7057 .
  
  dgn-gda:DGN32a31f45b08903b83b0d3259c13d7377 sio:SIO_000628 miriam-gene:6652, lld:C0521707;
    a sio:SIO_001121 .
}

dgn-np:NP376932.RAFg3R7C5nc2agNfzhWIWA9Z3R3LN4i50GaFbCCNbPRF0130_provenance {
  dgn-np:NP376932.RAFg3R7C5nc2agNfzhWIWA9Z3R3LN4i50GaFbCCNbPRF0130_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:NP376932.RAFg3R7C5nc2agNfzhWIWA9Z3R3LN4i50GaFbCCNbPRF0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:40+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" .
}