@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP734152.RAYHJM9I51NnjMKVcmZ4B8If_4lP8spOSpwHDxUQ6Pkus> .
@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:NP734152.RAYHJM9I51NnjMKVcmZ4B8If_4lP8spOSpwHDxUQ6Pkus130_head {
  this: np:hasAssertion dgn-np:NP734152.RAYHJM9I51NnjMKVcmZ4B8If_4lP8spOSpwHDxUQ6Pkus130_assertion ;
    np:hasProvenance dgn-np:NP734152.RAYHJM9I51NnjMKVcmZ4B8If_4lP8spOSpwHDxUQ6Pkus130_provenance ;
    np:hasPublicationInfo dgn-np:NP734152.RAYHJM9I51NnjMKVcmZ4B8If_4lP8spOSpwHDxUQ6Pkus130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP734152.RAYHJM9I51NnjMKVcmZ4B8If_4lP8spOSpwHDxUQ6Pkus130_provenance a np:Provenance .
  dgn-np:NP734152.RAYHJM9I51NnjMKVcmZ4B8If_4lP8spOSpwHDxUQ6Pkus130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP734152.RAYHJM9I51NnjMKVcmZ4B8If_4lP8spOSpwHDxUQ6Pkus130_assertion {
  miriam-gene:4858 a ncit:C16612 .
  lld:C0023462 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP734152.RAYHJM9I51NnjMKVcmZ4B8If_4lP8spOSpwHDxUQ6Pkus130_provenance {
  dgn-np:NP734152.RAYHJM9I51NnjMKVcmZ4B8If_4lP8spOSpwHDxUQ6Pkus130_assertion dcterms:description "[Application of our method to gene expression profiling for acute megakaryoblastic leukemia shows that our method detects an additional six genes, that are missed by both the standard ANOVA method as well as SVA, but may be relevant to this disease, as can be seen from mining the existing literature.]. 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:22238271 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
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dgn-np:NP734152.RAYHJM9I51NnjMKVcmZ4B8If_4lP8spOSpwHDxUQ6Pkus130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:25+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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}