@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP205994.RAHwYiggnKfIWDaHI6LYyFxCFZh4jE9_7CJOM9BRU2Xi0> .
@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:NP205994.RAHwYiggnKfIWDaHI6LYyFxCFZh4jE9_7CJOM9BRU2Xi0130_head {
  this: np:hasAssertion dgn-np:NP205994.RAHwYiggnKfIWDaHI6LYyFxCFZh4jE9_7CJOM9BRU2Xi0130_assertion ;
    np:hasProvenance dgn-np:NP205994.RAHwYiggnKfIWDaHI6LYyFxCFZh4jE9_7CJOM9BRU2Xi0130_provenance ;
    np:hasPublicationInfo dgn-np:NP205994.RAHwYiggnKfIWDaHI6LYyFxCFZh4jE9_7CJOM9BRU2Xi0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP205994.RAHwYiggnKfIWDaHI6LYyFxCFZh4jE9_7CJOM9BRU2Xi0130_assertion a np:Assertion .
  dgn-np:NP205994.RAHwYiggnKfIWDaHI6LYyFxCFZh4jE9_7CJOM9BRU2Xi0130_provenance a np:Provenance .
  dgn-np:NP205994.RAHwYiggnKfIWDaHI6LYyFxCFZh4jE9_7CJOM9BRU2Xi0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP205994.RAHwYiggnKfIWDaHI6LYyFxCFZh4jE9_7CJOM9BRU2Xi0130_assertion {
  miriam-gene:2146 a ncit:C16612 .
  lld:C3463824 a ncit:C7057 .
  dgn-gda:DGN9d56ac7d76cba05fac5b41d080e1ed7e sio:SIO_000628 miriam-gene:2146 , lld:C3463824 ;
    a sio:SIO_001121 .
}
dgn-np:NP205994.RAHwYiggnKfIWDaHI6LYyFxCFZh4jE9_7CJOM9BRU2Xi0130_provenance {
  dgn-np:NP205994.RAHwYiggnKfIWDaHI6LYyFxCFZh4jE9_7CJOM9BRU2Xi0130_assertion dcterms:description "[Aberrant differentiation in MDS can often be traced to abnormal DNA methylation (both gains and losses of DNA methylation genome wide and at specific loci) as well as mutations in genes that regulate epigenetic programs (TET2 and DNMT3a, both involved in DNA methylation control; EZH2 and ASXL1, both involved in histone methylation control).]. 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:23660859 ;
    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:NP205994.RAHwYiggnKfIWDaHI6LYyFxCFZh4jE9_7CJOM9BRU2Xi0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:53+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" .
}