@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP298687.RAprnN9fcIWle88CGF4gs2KFjncBqASirEckvUAMBhIpk> .
@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:NP298687.RAprnN9fcIWle88CGF4gs2KFjncBqASirEckvUAMBhIpk130_head {
  this: np:hasAssertion dgn-np:NP298687.RAprnN9fcIWle88CGF4gs2KFjncBqASirEckvUAMBhIpk130_assertion ;
    np:hasProvenance dgn-np:NP298687.RAprnN9fcIWle88CGF4gs2KFjncBqASirEckvUAMBhIpk130_provenance ;
    np:hasPublicationInfo dgn-np:NP298687.RAprnN9fcIWle88CGF4gs2KFjncBqASirEckvUAMBhIpk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP298687.RAprnN9fcIWle88CGF4gs2KFjncBqASirEckvUAMBhIpk130_assertion a np:Assertion .
  dgn-np:NP298687.RAprnN9fcIWle88CGF4gs2KFjncBqASirEckvUAMBhIpk130_provenance a np:Provenance .
  dgn-np:NP298687.RAprnN9fcIWle88CGF4gs2KFjncBqASirEckvUAMBhIpk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP298687.RAprnN9fcIWle88CGF4gs2KFjncBqASirEckvUAMBhIpk130_assertion {
  miriam-gene:4928 a ncit:C16612 .
  lld:C0026986 a ncit:C7057 .
  dgn-gda:DGN7f962d7d8469eea07eda64f5bb22ab41 sio:SIO_000628 miriam-gene:4928 , lld:C0026986 ;
    a sio:SIO_001121 .
}
dgn-np:NP298687.RAprnN9fcIWle88CGF4gs2KFjncBqASirEckvUAMBhIpk130_provenance {
  dgn-np:NP298687.RAprnN9fcIWle88CGF4gs2KFjncBqASirEckvUAMBhIpk130_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:NP298687.RAprnN9fcIWle88CGF4gs2KFjncBqASirEckvUAMBhIpk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:49+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" .
}