@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP631521.RA00YM5EaP68AOdEmMrh9ZecUlIoUY3MQl-OSslkg5WeM> .
@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:NP631521.RA00YM5EaP68AOdEmMrh9ZecUlIoUY3MQl-OSslkg5WeM130_head {
  this: np:hasAssertion dgn-np:NP631521.RA00YM5EaP68AOdEmMrh9ZecUlIoUY3MQl-OSslkg5WeM130_assertion;
    np:hasProvenance dgn-np:NP631521.RA00YM5EaP68AOdEmMrh9ZecUlIoUY3MQl-OSslkg5WeM130_provenance;
    np:hasPublicationInfo dgn-np:NP631521.RA00YM5EaP68AOdEmMrh9ZecUlIoUY3MQl-OSslkg5WeM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP631521.RA00YM5EaP68AOdEmMrh9ZecUlIoUY3MQl-OSslkg5WeM130_assertion a np:Assertion .
  
  dgn-np:NP631521.RA00YM5EaP68AOdEmMrh9ZecUlIoUY3MQl-OSslkg5WeM130_provenance a np:Provenance .
  
  dgn-np:NP631521.RA00YM5EaP68AOdEmMrh9ZecUlIoUY3MQl-OSslkg5WeM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP631521.RA00YM5EaP68AOdEmMrh9ZecUlIoUY3MQl-OSslkg5WeM130_assertion {
  miriam-gene:2512 a ncit:C16612 .
  
  lld:C1833213 a ncit:C7057 .
  
  dgn-gda:DGN67b4dd5cb02e2b324b02d05b0aa33a55 sio:SIO_000628 miriam-gene:2512, lld:C1833213;
    a sio:SIO_001121 .
}

dgn-np:NP631521.RA00YM5EaP68AOdEmMrh9ZecUlIoUY3MQl-OSslkg5WeM130_provenance {
  dgn-np:NP631521.RA00YM5EaP68AOdEmMrh9ZecUlIoUY3MQl-OSslkg5WeM130_assertion dcterms:description
      "[The data are consistent with robust transcription of FTL in the lens, and suggest that whereas variations clustered in the IRE of the FTL gene are directly associated with hereditary hyperferritinemia-cataract syndrome, such IRE variations are unlikely to play a significant role in the genetic etiology of age-related cataract.]. 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:23592921;
    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:NP631521.RA00YM5EaP68AOdEmMrh9ZecUlIoUY3MQl-OSslkg5WeM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:21+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" .
}