@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP694428.RAYKWh4QJk0t1XoJ81yF-TPjHm-ERrlIem2VbqstoKhQ8
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP694428.RAYKWh4QJk0t1XoJ81yF-TPjHm-ERrlIem2VbqstoKhQ8130_head
{
this:
np:hasAssertion
dgn-np:NP694428.RAYKWh4QJk0t1XoJ81yF-TPjHm-ERrlIem2VbqstoKhQ8130_assertion
;
np:hasProvenance
dgn-np:NP694428.RAYKWh4QJk0t1XoJ81yF-TPjHm-ERrlIem2VbqstoKhQ8130_provenance
;
np:hasPublicationInfo
dgn-np:NP694428.RAYKWh4QJk0t1XoJ81yF-TPjHm-ERrlIem2VbqstoKhQ8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP694428.RAYKWh4QJk0t1XoJ81yF-TPjHm-ERrlIem2VbqstoKhQ8130_assertion
a
np:Assertion
.
dgn-np:NP694428.RAYKWh4QJk0t1XoJ81yF-TPjHm-ERrlIem2VbqstoKhQ8130_provenance
a
np:Provenance
.
dgn-np:NP694428.RAYKWh4QJk0t1XoJ81yF-TPjHm-ERrlIem2VbqstoKhQ8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP694428.RAYKWh4QJk0t1XoJ81yF-TPjHm-ERrlIem2VbqstoKhQ8130_assertion
{
miriam-gene:4869
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGNf690b3aa576dfe36af2048a0a6928fd8
sio:SIO_000628
miriam-gene:4869
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP694428.RAYKWh4QJk0t1XoJ81yF-TPjHm-ERrlIem2VbqstoKhQ8130_provenance
{
dgn-np:NP694428.RAYKWh4QJk0t1XoJ81yF-TPjHm-ERrlIem2VbqstoKhQ8130_assertion
dcterms:description
"[To evaluate the prognostic significance of CEBPA mutations in the context of established molecular markers in cytogenetically normal (CN) acute myeloid leukemia (AML) and gain biologic insights into leukemogenesis of the CN-AML molecular high-risk subset (FLT3 internal tandem duplication [ITD] positive and/or NPM1 wild type) that has a significantly higher incidence of CEBPA mutations than the molecular low-risk subset (FLT3-ITD negative and NPM1 mutated).]. 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:18809607
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP694428.RAYKWh4QJk0t1XoJ81yF-TPjHm-ERrlIem2VbqstoKhQ8130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:00+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}