@prefix dc: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP7108.RAVmhu3iH4DXXE3CAzbuCk2STKHqe_GrGkSaBOqI7p9OA> .
@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 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:NP7108.RAVmhu3iH4DXXE3CAzbuCk2STKHqe_GrGkSaBOqI7p9OA130_head {
  this: np:hasAssertion dgn-np:NP7108.RAVmhu3iH4DXXE3CAzbuCk2STKHqe_GrGkSaBOqI7p9OA130_assertion;
    np:hasProvenance dgn-np:NP7108.RAVmhu3iH4DXXE3CAzbuCk2STKHqe_GrGkSaBOqI7p9OA130_provenance;
    np:hasPublicationInfo dgn-np:NP7108.RAVmhu3iH4DXXE3CAzbuCk2STKHqe_GrGkSaBOqI7p9OA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP7108.RAVmhu3iH4DXXE3CAzbuCk2STKHqe_GrGkSaBOqI7p9OA130_assertion a np:Assertion .
  
  dgn-np:NP7108.RAVmhu3iH4DXXE3CAzbuCk2STKHqe_GrGkSaBOqI7p9OA130_provenance a np:Provenance .
  
  dgn-np:NP7108.RAVmhu3iH4DXXE3CAzbuCk2STKHqe_GrGkSaBOqI7p9OA130_publicationInfo a np:PublicationInfo .
}

dgn-np:NP7108.RAVmhu3iH4DXXE3CAzbuCk2STKHqe_GrGkSaBOqI7p9OA130_assertion {
  miriam-gene:7486 a ncit:C16612 .
  
  lld:C0043119 a ncit:C7057 .
  
  dgn-gda:DGN63609371451deb6502c9328edd886691 sio:SIO_000628 miriam-gene:7486, lld:C0043119;
    a sio:SIO_001122 .
}

dgn-np:NP7108.RAVmhu3iH4DXXE3CAzbuCk2STKHqe_GrGkSaBOqI7p9OA130_provenance {
  dgn-np:NP7108.RAVmhu3iH4DXXE3CAzbuCk2STKHqe_GrGkSaBOqI7p9OA130_assertion dc:description
      "[The present communication summarizes, from among 99 WS subjects, the spectrum of 50 distinct mutations discovered by our group and by others since the WRN gene (also called RECQL2 or REQ3) was first cloned in 1996; 25 of these have not previously been published.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_curated;
    sio:SIO_000772 miriam-pubmed:16673358;
    prov:wasDerivedFrom dgn-void:uniprot-20130724;
    prov:wasGeneratedBy eco:ECO_0000218 .
  
  dgn-void:source_evidence_curated a eco:ECO_0000205;
    rdfs:comment "Gene-disease associations manually curated."@en;
    rdfs:label "DisGeNET evidence - CURATED"@en .
  
  dgn-void:uniprot-20130724 pav:importedOn "2013-07-24"^^xsd:date .
}

dgn-np:NP7108.RAVmhu3iH4DXXE3CAzbuCk2STKHqe_GrGkSaBOqI7p9OA130_publicationInfo {
  this: dc:created "2014-10-02T12:32:01+02:00"^^xsd:dateTime;
    dc:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dc:rightsHolder dgn-void:IBIGroup;
    dc: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" .
}