@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP336768.RACGC3DhCPP7aNeZTWztCBBnMzWQI_SIQoAG6m1Y1pwfg> .
@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:NP336768.RACGC3DhCPP7aNeZTWztCBBnMzWQI_SIQoAG6m1Y1pwfg130_head {
  this: np:hasAssertion dgn-np:NP336768.RACGC3DhCPP7aNeZTWztCBBnMzWQI_SIQoAG6m1Y1pwfg130_assertion;
    np:hasProvenance dgn-np:NP336768.RACGC3DhCPP7aNeZTWztCBBnMzWQI_SIQoAG6m1Y1pwfg130_provenance;
    np:hasPublicationInfo dgn-np:NP336768.RACGC3DhCPP7aNeZTWztCBBnMzWQI_SIQoAG6m1Y1pwfg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP336768.RACGC3DhCPP7aNeZTWztCBBnMzWQI_SIQoAG6m1Y1pwfg130_assertion a np:Assertion .
  
  dgn-np:NP336768.RACGC3DhCPP7aNeZTWztCBBnMzWQI_SIQoAG6m1Y1pwfg130_provenance a np:Provenance .
  
  dgn-np:NP336768.RACGC3DhCPP7aNeZTWztCBBnMzWQI_SIQoAG6m1Y1pwfg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP336768.RACGC3DhCPP7aNeZTWztCBBnMzWQI_SIQoAG6m1Y1pwfg130_assertion {
  miriam-gene:4928 a ncit:C16612 .
  
  lld:C0033027 a ncit:C7057 .
  
  dgn-gda:DGNc276c0c22250f1815e388fc63b24ae17 sio:SIO_000628 miriam-gene:4928, lld:C0033027;
    a sio:SIO_001121 .
}

dgn-np:NP336768.RACGC3DhCPP7aNeZTWztCBBnMzWQI_SIQoAG6m1Y1pwfg130_provenance {
  dgn-np:NP336768.RACGC3DhCPP7aNeZTWztCBBnMzWQI_SIQoAG6m1Y1pwfg130_assertion dcterms:description
      "[Using a NUP98-specific split-signal fluorescence in situ hybridization (FISH) probe combination, we analyzed 84 patients with acute myeloid leukemia (AML), acute lymphoblastic leukemia, or myelodysplastic syndrome with either normal karyotypes or 11p abnormalities to investigate whether there are unidentified 11p15 rearrangements.]. 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:16419055;
    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:NP336768.RACGC3DhCPP7aNeZTWztCBBnMzWQI_SIQoAG6m1Y1pwfg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:18+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" .
}