@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP556837.RANhHwsdtTEfMBdEqHfmJCSPSLd5GnzpDIEHkQ3lE2mbM> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP556837.RANhHwsdtTEfMBdEqHfmJCSPSLd5GnzpDIEHkQ3lE2mbM130_head {
  this: np:hasAssertion dgn-np:NP556837.RANhHwsdtTEfMBdEqHfmJCSPSLd5GnzpDIEHkQ3lE2mbM130_assertion;
    np:hasProvenance dgn-np:NP556837.RANhHwsdtTEfMBdEqHfmJCSPSLd5GnzpDIEHkQ3lE2mbM130_provenance;
    np:hasPublicationInfo dgn-np:NP556837.RANhHwsdtTEfMBdEqHfmJCSPSLd5GnzpDIEHkQ3lE2mbM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP556837.RANhHwsdtTEfMBdEqHfmJCSPSLd5GnzpDIEHkQ3lE2mbM130_assertion a np:Assertion .
  
  dgn-np:NP556837.RANhHwsdtTEfMBdEqHfmJCSPSLd5GnzpDIEHkQ3lE2mbM130_provenance a np:Provenance .
  
  dgn-np:NP556837.RANhHwsdtTEfMBdEqHfmJCSPSLd5GnzpDIEHkQ3lE2mbM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP556837.RANhHwsdtTEfMBdEqHfmJCSPSLd5GnzpDIEHkQ3lE2mbM130_assertion {
  miriam-gene:7486 a ncit:C16612 .
  
  lld:C0043119 a ncit:C7057 .
  
  dgn-gda:DGN1e27a66d06d9be96094f2d48f67b48e4 sio:SIO_000628 miriam-gene:7486, lld:C0043119;
    a sio:SIO_001121 .
}

dgn-np:NP556837.RANhHwsdtTEfMBdEqHfmJCSPSLd5GnzpDIEHkQ3lE2mbM130_provenance {
  dgn-np:NP556837.RANhHwsdtTEfMBdEqHfmJCSPSLd5GnzpDIEHkQ3lE2mbM130_assertion dcterms:description
      "[Werner syndrome (WS) is an autosomal recessive segmental progeroid syndrome caused by mutations in the Werner (WRN) gene leading to the early onset of many (but not all) aspects of normal aging.]. 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:16804003;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP556837.RANhHwsdtTEfMBdEqHfmJCSPSLd5GnzpDIEHkQ3lE2mbM130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:57+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}