@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP391757.RAbHHLORuoJJezQAmRgv9M1ldxmE-xRHVoY0nlWC1vQf0> .
@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:NP391757.RAbHHLORuoJJezQAmRgv9M1ldxmE-xRHVoY0nlWC1vQf0130_head {
  this: np:hasAssertion dgn-np:NP391757.RAbHHLORuoJJezQAmRgv9M1ldxmE-xRHVoY0nlWC1vQf0130_assertion ;
    np:hasProvenance dgn-np:NP391757.RAbHHLORuoJJezQAmRgv9M1ldxmE-xRHVoY0nlWC1vQf0130_provenance ;
    np:hasPublicationInfo dgn-np:NP391757.RAbHHLORuoJJezQAmRgv9M1ldxmE-xRHVoY0nlWC1vQf0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP391757.RAbHHLORuoJJezQAmRgv9M1ldxmE-xRHVoY0nlWC1vQf0130_assertion a np:Assertion .
  dgn-np:NP391757.RAbHHLORuoJJezQAmRgv9M1ldxmE-xRHVoY0nlWC1vQf0130_provenance a np:Provenance .
  dgn-np:NP391757.RAbHHLORuoJJezQAmRgv9M1ldxmE-xRHVoY0nlWC1vQf0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP391757.RAbHHLORuoJJezQAmRgv9M1ldxmE-xRHVoY0nlWC1vQf0130_assertion {
  miriam-gene:1788 a ncit:C16612 .
  lld:C0007097 a ncit:C7057 .
  dgn-gda:DGN270b5ea7881c547002d89fb14b01ad33 sio:SIO_000628 miriam-gene:1788 , lld:C0007097 ;
    a sio:SIO_001121 .
}
dgn-np:NP391757.RAbHHLORuoJJezQAmRgv9M1ldxmE-xRHVoY0nlWC1vQf0130_provenance {
  dgn-np:NP391757.RAbHHLORuoJJezQAmRgv9M1ldxmE-xRHVoY0nlWC1vQf0130_assertion dcterms:description "[To see whether DNMT3A mutation occurs in other malignancies as well, we analyzed DNMT3A in 916 cancer tissues from 401 hematologic malignancies (AML, acute lymphoblastic leukemias (ALL), multiple myelomas and lymphomas) and 515 carcinomas (lung, breast, prostate, colorectal and gastric carcinomas) using a single-strand conformation polymorphism (SSCP) assay.]. 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:23031157 ;
    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:NP391757.RAbHHLORuoJJezQAmRgv9M1ldxmE-xRHVoY0nlWC1vQf0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:53+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" .
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}