@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP439008.RAtoXvHe5hBSiLaVmk2NOEW3iZaWia4vzZLNjN_4rFJ9A
> .
@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:NP439008.RAtoXvHe5hBSiLaVmk2NOEW3iZaWia4vzZLNjN_4rFJ9A130_head
{
this:
np:hasAssertion
dgn-np:NP439008.RAtoXvHe5hBSiLaVmk2NOEW3iZaWia4vzZLNjN_4rFJ9A130_assertion
;
np:hasProvenance
dgn-np:NP439008.RAtoXvHe5hBSiLaVmk2NOEW3iZaWia4vzZLNjN_4rFJ9A130_provenance
;
np:hasPublicationInfo
dgn-np:NP439008.RAtoXvHe5hBSiLaVmk2NOEW3iZaWia4vzZLNjN_4rFJ9A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP439008.RAtoXvHe5hBSiLaVmk2NOEW3iZaWia4vzZLNjN_4rFJ9A130_assertion
a
np:Assertion
.
dgn-np:NP439008.RAtoXvHe5hBSiLaVmk2NOEW3iZaWia4vzZLNjN_4rFJ9A130_provenance
a
np:Provenance
.
dgn-np:NP439008.RAtoXvHe5hBSiLaVmk2NOEW3iZaWia4vzZLNjN_4rFJ9A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP439008.RAtoXvHe5hBSiLaVmk2NOEW3iZaWia4vzZLNjN_4rFJ9A130_assertion
{
miriam-gene:3757
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGN5b54ad53fbe628995ddf3ad707c9fc14
sio:SIO_000628
miriam-gene:3757
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP439008.RAtoXvHe5hBSiLaVmk2NOEW3iZaWia4vzZLNjN_4rFJ9A130_provenance
{
dgn-np:NP439008.RAtoXvHe5hBSiLaVmk2NOEW3iZaWia4vzZLNjN_4rFJ9A130_assertion
dcterms:description
"[Mutation status of FLT3, NPM1, CEBPA, and WT1 genes and gene expression levels of ERG, MN1, BAALC, FLT3, and WT1 have been identified as possible prognostic markers in acute myeloid leukemia (AML).]. 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:21967978
;
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:NP439008.RAtoXvHe5hBSiLaVmk2NOEW3iZaWia4vzZLNjN_4rFJ9A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:19+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" .
}