@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP606009.RA1f42WXh-CCRHyaFMTjkEe8HozxBKbqvKKAT-p2rNkd0> .
@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/v3.0.0/void/> .

dgn-np:NP606009.RA1f42WXh-CCRHyaFMTjkEe8HozxBKbqvKKAT-p2rNkd0130_head {
  this: np:hasAssertion dgn-np:NP606009.RA1f42WXh-CCRHyaFMTjkEe8HozxBKbqvKKAT-p2rNkd0130_assertion;
    np:hasProvenance dgn-np:NP606009.RA1f42WXh-CCRHyaFMTjkEe8HozxBKbqvKKAT-p2rNkd0130_provenance;
    np:hasPublicationInfo dgn-np:NP606009.RA1f42WXh-CCRHyaFMTjkEe8HozxBKbqvKKAT-p2rNkd0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP606009.RA1f42WXh-CCRHyaFMTjkEe8HozxBKbqvKKAT-p2rNkd0130_assertion a np:Assertion .
  
  dgn-np:NP606009.RA1f42WXh-CCRHyaFMTjkEe8HozxBKbqvKKAT-p2rNkd0130_provenance a np:Provenance .
  
  dgn-np:NP606009.RA1f42WXh-CCRHyaFMTjkEe8HozxBKbqvKKAT-p2rNkd0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP606009.RA1f42WXh-CCRHyaFMTjkEe8HozxBKbqvKKAT-p2rNkd0130_assertion {
  miriam-gene:5048 a ncit:C16612 .
  
  lld:C0027671 a ncit:C7057 .
  
  dgn-gda:DGNabb6dc87f795f0d46df316fa927a7fb4 sio:SIO_000628 miriam-gene:5048, lld:C0027671;
    a sio:SIO_001121 .
}

dgn-np:NP606009.RA1f42WXh-CCRHyaFMTjkEe8HozxBKbqvKKAT-p2rNkd0130_provenance {
  dgn-np:NP606009.RA1f42WXh-CCRHyaFMTjkEe8HozxBKbqvKKAT-p2rNkd0130_assertion dcterms:description
      "[Furthermore cytogenetic studies are warranted in larger groups of MDS cases to identify newly acquired chromosome aberrations that may aid in cloning new genes involved in the neoplastic process, ultimately helping in the development of targeted therapeutic drugs.]. 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:21193364;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP606009.RA1f42WXh-CCRHyaFMTjkEe8HozxBKbqvKKAT-p2rNkd0130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:42+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}