@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP242037.RAu_VhA0LyVRqOvEAztKQz-nlBFKSAkHI8dBfiP8OH04E> .
@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:NP242037.RAu_VhA0LyVRqOvEAztKQz-nlBFKSAkHI8dBfiP8OH04E130_head {
  this: np:hasAssertion dgn-np:NP242037.RAu_VhA0LyVRqOvEAztKQz-nlBFKSAkHI8dBfiP8OH04E130_assertion;
    np:hasProvenance dgn-np:NP242037.RAu_VhA0LyVRqOvEAztKQz-nlBFKSAkHI8dBfiP8OH04E130_provenance;
    np:hasPublicationInfo dgn-np:NP242037.RAu_VhA0LyVRqOvEAztKQz-nlBFKSAkHI8dBfiP8OH04E130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP242037.RAu_VhA0LyVRqOvEAztKQz-nlBFKSAkHI8dBfiP8OH04E130_assertion a np:Assertion .
  
  dgn-np:NP242037.RAu_VhA0LyVRqOvEAztKQz-nlBFKSAkHI8dBfiP8OH04E130_provenance a np:Provenance .
  
  dgn-np:NP242037.RAu_VhA0LyVRqOvEAztKQz-nlBFKSAkHI8dBfiP8OH04E130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP242037.RAu_VhA0LyVRqOvEAztKQz-nlBFKSAkHI8dBfiP8OH04E130_assertion {
  miriam-gene:7301 a ncit:C16612 .
  
  lld:C0023449 a ncit:C7057 .
  
  dgn-gda:DGN21047f2325719c58dad99f829e5ed8ed sio:SIO_000628 miriam-gene:7301, lld:C0023449;
    a sio:SIO_001121 .
}

dgn-np:NP242037.RAu_VhA0LyVRqOvEAztKQz-nlBFKSAkHI8dBfiP8OH04E130_provenance {
  dgn-np:NP242037.RAu_VhA0LyVRqOvEAztKQz-nlBFKSAkHI8dBfiP8OH04E130_assertion dcterms:description
      "[Spectral karyotyping (SKY) on metaphase spreads from 15 high hyperdiploid (>51 chromosomes) childhood acute lymphoblastic leukemias (ALL), which typically display a poor chromosome morphology, was performed in order to investigate the pattern of numerical abnormalities, reveal the chromosomal origin of marker chromosomes, and identify translocations and other interchromosomal rearrangements not detected by G-banding analysis.]. 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:11422408;
    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:NP242037.RAu_VhA0LyVRqOvEAztKQz-nlBFKSAkHI8dBfiP8OH04E130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:15+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" .
}