@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP193508.RACuWyfVLgNIBPBugvpVlYtND_eT4qYlEdUFOGAxp-jP4
> .
@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:NP193508.RACuWyfVLgNIBPBugvpVlYtND_eT4qYlEdUFOGAxp-jP4130_head
{
this:
np:hasAssertion
dgn-np:NP193508.RACuWyfVLgNIBPBugvpVlYtND_eT4qYlEdUFOGAxp-jP4130_assertion
;
np:hasProvenance
dgn-np:NP193508.RACuWyfVLgNIBPBugvpVlYtND_eT4qYlEdUFOGAxp-jP4130_provenance
;
np:hasPublicationInfo
dgn-np:NP193508.RACuWyfVLgNIBPBugvpVlYtND_eT4qYlEdUFOGAxp-jP4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP193508.RACuWyfVLgNIBPBugvpVlYtND_eT4qYlEdUFOGAxp-jP4130_assertion
a
np:Assertion
.
dgn-np:NP193508.RACuWyfVLgNIBPBugvpVlYtND_eT4qYlEdUFOGAxp-jP4130_provenance
a
np:Provenance
.
dgn-np:NP193508.RACuWyfVLgNIBPBugvpVlYtND_eT4qYlEdUFOGAxp-jP4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP193508.RACuWyfVLgNIBPBugvpVlYtND_eT4qYlEdUFOGAxp-jP4130_assertion
{
miriam-gene:4330
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGN0f59fbdc7e32edad7f5d7ca7ed268ca1
sio:SIO_000628
miriam-gene:4330
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP193508.RACuWyfVLgNIBPBugvpVlYtND_eT4qYlEdUFOGAxp-jP4130_provenance
{
dgn-np:NP193508.RACuWyfVLgNIBPBugvpVlYtND_eT4qYlEdUFOGAxp-jP4130_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:NP193508.RACuWyfVLgNIBPBugvpVlYtND_eT4qYlEdUFOGAxp-jP4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:46+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" .
}