@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP643419.RALPO4-Lpq2tOEDaf7FBgb3hRNuBTEFfKJM6gVOUDQdFw> .
@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:NP643419.RALPO4-Lpq2tOEDaf7FBgb3hRNuBTEFfKJM6gVOUDQdFw130_head {
  this: np:hasAssertion dgn-np:NP643419.RALPO4-Lpq2tOEDaf7FBgb3hRNuBTEFfKJM6gVOUDQdFw130_assertion ;
    np:hasProvenance dgn-np:NP643419.RALPO4-Lpq2tOEDaf7FBgb3hRNuBTEFfKJM6gVOUDQdFw130_provenance ;
    np:hasPublicationInfo dgn-np:NP643419.RALPO4-Lpq2tOEDaf7FBgb3hRNuBTEFfKJM6gVOUDQdFw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP643419.RALPO4-Lpq2tOEDaf7FBgb3hRNuBTEFfKJM6gVOUDQdFw130_assertion a np:Assertion .
  dgn-np:NP643419.RALPO4-Lpq2tOEDaf7FBgb3hRNuBTEFfKJM6gVOUDQdFw130_provenance a np:Provenance .
  dgn-np:NP643419.RALPO4-Lpq2tOEDaf7FBgb3hRNuBTEFfKJM6gVOUDQdFw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP643419.RALPO4-Lpq2tOEDaf7FBgb3hRNuBTEFfKJM6gVOUDQdFw130_assertion {
  miriam-gene:2322 a ncit:C16612 .
  lld:C1961099 a ncit:C7057 .
  dgn-gda:DGN7b517f02c14b29eae94bbfbe25b237ea sio:SIO_000628 miriam-gene:2322 , lld:C1961099 ;
    a sio:SIO_001121 .
}
dgn-np:NP643419.RALPO4-Lpq2tOEDaf7FBgb3hRNuBTEFfKJM6gVOUDQdFw130_provenance {
  dgn-np:NP643419.RALPO4-Lpq2tOEDaf7FBgb3hRNuBTEFfKJM6gVOUDQdFw130_assertion dcterms:description "[For practical clinical use, GE profiling of precursor B acute lymphoblastic leukemia, precursor T acute lymphoblastic leukemia, and acute myeloid leukemia has supported most of the information that has been obtained by cytogenetic and molecular studies (except for the identification of FLT3 mutations for molecular analysis), but extrapolation of the analyses leaves much to be gained based on the GE profiling data.]. 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:16594743 ;
    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:NP643419.RALPO4-Lpq2tOEDaf7FBgb3hRNuBTEFfKJM6gVOUDQdFw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:28+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" .
}