@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP520567.RAvp6kVRB1WQzN-E6YLDNicRf9iGopHa85H9wVYT61mvs
> .
@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:NP520567.RAvp6kVRB1WQzN-E6YLDNicRf9iGopHa85H9wVYT61mvs130_head
{
this:
np:hasAssertion
dgn-np:NP520567.RAvp6kVRB1WQzN-E6YLDNicRf9iGopHa85H9wVYT61mvs130_assertion
;
np:hasProvenance
dgn-np:NP520567.RAvp6kVRB1WQzN-E6YLDNicRf9iGopHa85H9wVYT61mvs130_provenance
;
np:hasPublicationInfo
dgn-np:NP520567.RAvp6kVRB1WQzN-E6YLDNicRf9iGopHa85H9wVYT61mvs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP520567.RAvp6kVRB1WQzN-E6YLDNicRf9iGopHa85H9wVYT61mvs130_assertion
a
np:Assertion
.
dgn-np:NP520567.RAvp6kVRB1WQzN-E6YLDNicRf9iGopHa85H9wVYT61mvs130_provenance
a
np:Provenance
.
dgn-np:NP520567.RAvp6kVRB1WQzN-E6YLDNicRf9iGopHa85H9wVYT61mvs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP520567.RAvp6kVRB1WQzN-E6YLDNicRf9iGopHa85H9wVYT61mvs130_assertion
{
miriam-gene:1050
a
ncit:C16612
.
lld:C0598766
a
ncit:C7057
.
dgn-gda:DGN20ddb6d66b5bf34df755930cf7e1cd77
sio:SIO_000628
miriam-gene:1050
,
lld:C0598766
;
a
sio:SIO_001121
.
}
dgn-np:NP520567.RAvp6kVRB1WQzN-E6YLDNicRf9iGopHa85H9wVYT61mvs130_provenance
{
dgn-np:NP520567.RAvp6kVRB1WQzN-E6YLDNicRf9iGopHa85H9wVYT61mvs130_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-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:NP520567.RAvp6kVRB1WQzN-E6YLDNicRf9iGopHa85H9wVYT61mvs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:10+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" .
}