@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP266670.RAGSvQ7cQWufkJ6kFRF4sbp8Qdoa8UsZf5Q2RrkG4kUKY> .
@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:NP266670.RAGSvQ7cQWufkJ6kFRF4sbp8Qdoa8UsZf5Q2RrkG4kUKY130_head {
  this: np:hasAssertion dgn-np:NP266670.RAGSvQ7cQWufkJ6kFRF4sbp8Qdoa8UsZf5Q2RrkG4kUKY130_assertion;
    np:hasProvenance dgn-np:NP266670.RAGSvQ7cQWufkJ6kFRF4sbp8Qdoa8UsZf5Q2RrkG4kUKY130_provenance;
    np:hasPublicationInfo dgn-np:NP266670.RAGSvQ7cQWufkJ6kFRF4sbp8Qdoa8UsZf5Q2RrkG4kUKY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP266670.RAGSvQ7cQWufkJ6kFRF4sbp8Qdoa8UsZf5Q2RrkG4kUKY130_assertion a np:Assertion .
  
  dgn-np:NP266670.RAGSvQ7cQWufkJ6kFRF4sbp8Qdoa8UsZf5Q2RrkG4kUKY130_provenance a np:Provenance .
  
  dgn-np:NP266670.RAGSvQ7cQWufkJ6kFRF4sbp8Qdoa8UsZf5Q2RrkG4kUKY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP266670.RAGSvQ7cQWufkJ6kFRF4sbp8Qdoa8UsZf5Q2RrkG4kUKY130_assertion {
  miriam-gene:9244 a ncit:C16612 .
  
  lld:C0023487 a ncit:C7057 .
  
  dgn-gda:DGN41016afc48147277d8e3931435e84e0e sio:SIO_000628 miriam-gene:9244, lld:C0023487;
    a sio:SIO_001121 .
}

dgn-np:NP266670.RAGSvQ7cQWufkJ6kFRF4sbp8Qdoa8UsZf5Q2RrkG4kUKY130_provenance {
  dgn-np:NP266670.RAGSvQ7cQWufkJ6kFRF4sbp8Qdoa8UsZf5Q2RrkG4kUKY130_assertion dcterms:description
      "[Chromosomal in situ suppression (CISS) hybridization was performed with library DNA from sorted human chromosomes 8, 9, 15, 17, 21, and 22 on immunologically stained bone marrow cells of four patients with a hematologic neoplasm, including two patients with myelodysplastic syndrome and trisomy 8, one patient with promyelocytic leukemia bearing the translocation t(15;17)(q22;q11-12), and one patient with chronic myeloid leukemia and the translocation t(9;22)(q34;q11).]. 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:1373313;
    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:NP266670.RAGSvQ7cQWufkJ6kFRF4sbp8Qdoa8UsZf5Q2RrkG4kUKY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:29+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" .
}