@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP850036.RADbqV2vqnu7sac_4erFymPXFMb8qeLbGxB0qvJgtBCyU
> .
@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/v3.0.0/void/
> .
dgn-np:NP850036.RADbqV2vqnu7sac_4erFymPXFMb8qeLbGxB0qvJgtBCyU130_head
{
this:
np:hasAssertion
dgn-np:NP850036.RADbqV2vqnu7sac_4erFymPXFMb8qeLbGxB0qvJgtBCyU130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP850036.RADbqV2vqnu7sac_4erFymPXFMb8qeLbGxB0qvJgtBCyU130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP850036.RADbqV2vqnu7sac_4erFymPXFMb8qeLbGxB0qvJgtBCyU130_assertion
a
np:Assertion
.
dgn-np:NP850036.RADbqV2vqnu7sac_4erFymPXFMb8qeLbGxB0qvJgtBCyU130_provenance
a
np:Provenance
.
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a
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{
miriam-gene:10660
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGNafbb83baa62a080b214a3f6c1ac6e425
sio:SIO_000628
miriam-gene:10660
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP850036.RADbqV2vqnu7sac_4erFymPXFMb8qeLbGxB0qvJgtBCyU130_provenance
{
dgn-np:NP850036.RADbqV2vqnu7sac_4erFymPXFMb8qeLbGxB0qvJgtBCyU130_assertion
dcterms:description
"[With respect to gene expression profiling, we show that AML cases with an NPM1 mutation cluster in specific subtypes of AML with previously established gene expression signatures, are highly associated with a homeobox gene-specific expression signature, and can be predicted with high accuracy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:16109776
;
prov:wasDerivedFrom
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;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP850036.RADbqV2vqnu7sac_4erFymPXFMb8qeLbGxB0qvJgtBCyU130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:46:16+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
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;
pav:authoredBy
<
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> , <
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> , <
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> , <
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
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pav:version
"v3.0.0" .
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