@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP436477.RAI0pWeT5UkFSUGrGfsEYA3CkmtiLbiLMJiqguTjkhLuE> .
@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:NP436477.RAI0pWeT5UkFSUGrGfsEYA3CkmtiLbiLMJiqguTjkhLuE130_head {
  this: np:hasAssertion dgn-np:NP436477.RAI0pWeT5UkFSUGrGfsEYA3CkmtiLbiLMJiqguTjkhLuE130_assertion ;
    np:hasProvenance dgn-np:NP436477.RAI0pWeT5UkFSUGrGfsEYA3CkmtiLbiLMJiqguTjkhLuE130_provenance ;
    np:hasPublicationInfo dgn-np:NP436477.RAI0pWeT5UkFSUGrGfsEYA3CkmtiLbiLMJiqguTjkhLuE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP436477.RAI0pWeT5UkFSUGrGfsEYA3CkmtiLbiLMJiqguTjkhLuE130_assertion a np:Assertion .
  dgn-np:NP436477.RAI0pWeT5UkFSUGrGfsEYA3CkmtiLbiLMJiqguTjkhLuE130_provenance a np:Provenance .
  dgn-np:NP436477.RAI0pWeT5UkFSUGrGfsEYA3CkmtiLbiLMJiqguTjkhLuE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP436477.RAI0pWeT5UkFSUGrGfsEYA3CkmtiLbiLMJiqguTjkhLuE130_assertion {
  miriam-gene:4869 a ncit:C16612 .
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    a sio:SIO_001121 .
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dgn-np:NP436477.RAI0pWeT5UkFSUGrGfsEYA3CkmtiLbiLMJiqguTjkhLuE130_provenance {
  dgn-np:NP436477.RAI0pWeT5UkFSUGrGfsEYA3CkmtiLbiLMJiqguTjkhLuE130_assertion dcterms:description "[As far as we know, this is the first report of NPM1 mutation in patients with MDS in the English literature until now, and our primary data support that NPM1 mutations may be also involved in the pathogenesis of MDS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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    prov:wasDerivedFrom dgn-void:befree-20140225 ;
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
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dgn-np:NP436477.RAI0pWeT5UkFSUGrGfsEYA3CkmtiLbiLMJiqguTjkhLuE130_publicationInfo {
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    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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}