@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP231320.RArg6l5qFWGxlzNq-vR1s_Dsj7Sa9QKqSY6WCpaAHKDpw> .
@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:NP231320.RArg6l5qFWGxlzNq-vR1s_Dsj7Sa9QKqSY6WCpaAHKDpw130_head {
  this: np:hasAssertion dgn-np:NP231320.RArg6l5qFWGxlzNq-vR1s_Dsj7Sa9QKqSY6WCpaAHKDpw130_assertion ;
    np:hasProvenance dgn-np:NP231320.RArg6l5qFWGxlzNq-vR1s_Dsj7Sa9QKqSY6WCpaAHKDpw130_provenance ;
    np:hasPublicationInfo dgn-np:NP231320.RArg6l5qFWGxlzNq-vR1s_Dsj7Sa9QKqSY6WCpaAHKDpw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP231320.RArg6l5qFWGxlzNq-vR1s_Dsj7Sa9QKqSY6WCpaAHKDpw130_assertion a np:Assertion .
  dgn-np:NP231320.RArg6l5qFWGxlzNq-vR1s_Dsj7Sa9QKqSY6WCpaAHKDpw130_provenance a np:Provenance .
  dgn-np:NP231320.RArg6l5qFWGxlzNq-vR1s_Dsj7Sa9QKqSY6WCpaAHKDpw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP231320.RArg6l5qFWGxlzNq-vR1s_Dsj7Sa9QKqSY6WCpaAHKDpw130_assertion {
  miriam-gene:2187 a ncit:C16612 .
  lld:C0013080 a ncit:C7057 .
  dgn-gda:DGNb739f200fbb30808a8278034427a6d29 sio:SIO_000628 miriam-gene:2187 , lld:C0013080 ;
    a sio:SIO_001121 .
}
dgn-np:NP231320.RArg6l5qFWGxlzNq-vR1s_Dsj7Sa9QKqSY6WCpaAHKDpw130_provenance {
  dgn-np:NP231320.RArg6l5qFWGxlzNq-vR1s_Dsj7Sa9QKqSY6WCpaAHKDpw130_assertion dcterms:description "[Although the cause of leukaemia in Down syndrome (DS) remains unknown, potential candidate genes include the ones on chromosome 21, and in particular AML1, the rearrangement of which in the t(8,21) is associated with the French-American-British (FAB) classification M2 subtype of acute myeloid leukaemia (AML) in the general population and has been described in Down patients with AML-M2.]. 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:9177434 ;
    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:NP231320.RArg6l5qFWGxlzNq-vR1s_Dsj7Sa9QKqSY6WCpaAHKDpw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:09+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" .
}