@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP783818.RAjNQzzrd8rnjSSOvblOioj2M6v_cSb7E-gi07JXEix_s> .
@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:NP783818.RAjNQzzrd8rnjSSOvblOioj2M6v_cSb7E-gi07JXEix_s130_head {
  this: np:hasAssertion dgn-np:NP783818.RAjNQzzrd8rnjSSOvblOioj2M6v_cSb7E-gi07JXEix_s130_assertion;
    np:hasProvenance dgn-np:NP783818.RAjNQzzrd8rnjSSOvblOioj2M6v_cSb7E-gi07JXEix_s130_provenance;
    np:hasPublicationInfo dgn-np:NP783818.RAjNQzzrd8rnjSSOvblOioj2M6v_cSb7E-gi07JXEix_s130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP783818.RAjNQzzrd8rnjSSOvblOioj2M6v_cSb7E-gi07JXEix_s130_assertion a np:Assertion .
  
  dgn-np:NP783818.RAjNQzzrd8rnjSSOvblOioj2M6v_cSb7E-gi07JXEix_s130_provenance a np:Provenance .
  
  dgn-np:NP783818.RAjNQzzrd8rnjSSOvblOioj2M6v_cSb7E-gi07JXEix_s130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP783818.RAjNQzzrd8rnjSSOvblOioj2M6v_cSb7E-gi07JXEix_s130_assertion {
  miriam-gene:3342 a ncit:C16612 .
  
  lld:C0026948 a ncit:C7057 .
  
  dgn-gda:DGN4d1e8b8405c21cea88f326e1a878e8cc sio:SIO_000628 miriam-gene:3342, lld:C0026948;
    a sio:SIO_001121 .
}

dgn-np:NP783818.RAjNQzzrd8rnjSSOvblOioj2M6v_cSb7E-gi07JXEix_s130_provenance {
  dgn-np:NP783818.RAjNQzzrd8rnjSSOvblOioj2M6v_cSb7E-gi07JXEix_s130_assertion dcterms:description
      "[We analysed 18 cases of Sézary syndrome (SS) and 16 cases of mycosis fungoides (MF) by comparative genomic hybridization (CGH) analysis, and correlated findings with the results of additional conventional cytogenetics, fluorescent in situ hybridization (FISH) and allelotyping studies.]. 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:12207585;
    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:NP783818.RAjNQzzrd8rnjSSOvblOioj2M6v_cSb7E-gi07JXEix_s130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:55+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" .
}