@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP419248.RAK1B3mgB7_7fNj-gyCVuJnm68K_hV0F8eOaXPLI9M248
> .
@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:NP419248.RAK1B3mgB7_7fNj-gyCVuJnm68K_hV0F8eOaXPLI9M248130_head
{
this:
np:hasAssertion
dgn-np:NP419248.RAK1B3mgB7_7fNj-gyCVuJnm68K_hV0F8eOaXPLI9M248130_assertion
;
np:hasProvenance
dgn-np:NP419248.RAK1B3mgB7_7fNj-gyCVuJnm68K_hV0F8eOaXPLI9M248130_provenance
;
np:hasPublicationInfo
dgn-np:NP419248.RAK1B3mgB7_7fNj-gyCVuJnm68K_hV0F8eOaXPLI9M248130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP419248.RAK1B3mgB7_7fNj-gyCVuJnm68K_hV0F8eOaXPLI9M248130_assertion
a
np:Assertion
.
dgn-np:NP419248.RAK1B3mgB7_7fNj-gyCVuJnm68K_hV0F8eOaXPLI9M248130_provenance
a
np:Provenance
.
dgn-np:NP419248.RAK1B3mgB7_7fNj-gyCVuJnm68K_hV0F8eOaXPLI9M248130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP419248.RAK1B3mgB7_7fNj-gyCVuJnm68K_hV0F8eOaXPLI9M248130_assertion
{
miriam-gene:4330
a
ncit:C16612
.
lld:C0026986
a
ncit:C7057
.
dgn-gda:DGNd27b6115c20bd29e9fbcc4e7c9038577
sio:SIO_000628
miriam-gene:4330
,
lld:C0026986
;
a
sio:SIO_001121
.
}
dgn-np:NP419248.RAK1B3mgB7_7fNj-gyCVuJnm68K_hV0F8eOaXPLI9M248130_provenance
{
dgn-np:NP419248.RAK1B3mgB7_7fNj-gyCVuJnm68K_hV0F8eOaXPLI9M248130_assertion
dcterms:description
"[Overexpression of MN1, ERG, BAALC, and EVI1 (MEBE) genes in cytogenetically normal acute myeloid leukemia (AML) patients is associated with poor prognosis, but their prognostic effect in patients with myelodysplastic syndromes (MDS) has not been studied systematically.]. 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:22488406
;
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:NP419248.RAK1B3mgB7_7fNj-gyCVuJnm68K_hV0F8eOaXPLI9M248130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:09+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" .
}