@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP696059.RAyn_fd_DBIRAaHE6kNMFzcDljtA4zg48c-52FbWCEocA> .
@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:NP696059.RAyn_fd_DBIRAaHE6kNMFzcDljtA4zg48c-52FbWCEocA130_head {
  this: np:hasAssertion dgn-np:NP696059.RAyn_fd_DBIRAaHE6kNMFzcDljtA4zg48c-52FbWCEocA130_assertion;
    np:hasProvenance dgn-np:NP696059.RAyn_fd_DBIRAaHE6kNMFzcDljtA4zg48c-52FbWCEocA130_provenance;
    np:hasPublicationInfo dgn-np:NP696059.RAyn_fd_DBIRAaHE6kNMFzcDljtA4zg48c-52FbWCEocA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP696059.RAyn_fd_DBIRAaHE6kNMFzcDljtA4zg48c-52FbWCEocA130_assertion a np:Assertion .
  
  dgn-np:NP696059.RAyn_fd_DBIRAaHE6kNMFzcDljtA4zg48c-52FbWCEocA130_provenance a np:Provenance .
  
  dgn-np:NP696059.RAyn_fd_DBIRAaHE6kNMFzcDljtA4zg48c-52FbWCEocA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP696059.RAyn_fd_DBIRAaHE6kNMFzcDljtA4zg48c-52FbWCEocA130_assertion {
  miriam-gene:924 a ncit:C16612 .
  
  lld:C0036920 a ncit:C7057 .
  
  dgn-gda:DGNa3e11e80df35462ddfb53d19eabd0a7d sio:SIO_000628 miriam-gene:924, lld:C0036920;
    a sio:SIO_001121 .
}

dgn-np:NP696059.RAyn_fd_DBIRAaHE6kNMFzcDljtA4zg48c-52FbWCEocA130_provenance {
  dgn-np:NP696059.RAyn_fd_DBIRAaHE6kNMFzcDljtA4zg48c-52FbWCEocA130_assertion dcterms:description
      "[High-level expression of c-myb in the peripheral blood as assessed by quantitative RT-PCR constitutes an additional diagnostic parameter for SS and may be especially useful in cases in which morphological determination of Sézary cells or FACS analysis of CD7 and CD26 remain inconclusive.]. 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:16088151;
    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:NP696059.RAyn_fd_DBIRAaHE6kNMFzcDljtA4zg48c-52FbWCEocA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:03+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" .
}