@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP266665.RAOxyLUJ1jKO99iITCpjVG9i0D-d5Hi-UzFaDC8cC-I-Q> .
@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:NP266665.RAOxyLUJ1jKO99iITCpjVG9i0D-d5Hi-UzFaDC8cC-I-Q130_head {
  this: np:hasAssertion dgn-np:NP266665.RAOxyLUJ1jKO99iITCpjVG9i0D-d5Hi-UzFaDC8cC-I-Q130_assertion;
    np:hasProvenance dgn-np:NP266665.RAOxyLUJ1jKO99iITCpjVG9i0D-d5Hi-UzFaDC8cC-I-Q130_provenance;
    np:hasPublicationInfo dgn-np:NP266665.RAOxyLUJ1jKO99iITCpjVG9i0D-d5Hi-UzFaDC8cC-I-Q130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP266665.RAOxyLUJ1jKO99iITCpjVG9i0D-d5Hi-UzFaDC8cC-I-Q130_assertion a np:Assertion .
  
  dgn-np:NP266665.RAOxyLUJ1jKO99iITCpjVG9i0D-d5Hi-UzFaDC8cC-I-Q130_provenance a np:Provenance .
  
  dgn-np:NP266665.RAOxyLUJ1jKO99iITCpjVG9i0D-d5Hi-UzFaDC8cC-I-Q130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP266665.RAOxyLUJ1jKO99iITCpjVG9i0D-d5Hi-UzFaDC8cC-I-Q130_assertion {
  miriam-gene:2187 a ncit:C16612 .
  
  lld:C1961102 a ncit:C7057 .
  
  dgn-gda:DGNedeb9ccaf150e5cc367c77f13b141e0a sio:SIO_000628 miriam-gene:2187, lld:C1961102;
    a sio:SIO_001121 .
}

dgn-np:NP266665.RAOxyLUJ1jKO99iITCpjVG9i0D-d5Hi-UzFaDC8cC-I-Q130_provenance {
  dgn-np:NP266665.RAOxyLUJ1jKO99iITCpjVG9i0D-d5Hi-UzFaDC8cC-I-Q130_assertion dcterms:description
      "[The distinct protein profiles of acute leukemia FAB types or subtypes were successfully explored, including acute myeloid leukemia (AML), its subtypes (M2, M3, and M5) and acute lymphoid leukemia (ALL), which were homogeneous within substantial samples of the respective subgroups but clearly differed from all other subgroups.]. 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:15501966;
    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:NP266665.RAOxyLUJ1jKO99iITCpjVG9i0D-d5Hi-UzFaDC8cC-I-Q130_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" .
}