@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP648123.RApxXth5RgTY7Eb9Y1cv7jSxPlREt8r5JzWJh2BPlJjuI
> .
@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:NP648123.RApxXth5RgTY7Eb9Y1cv7jSxPlREt8r5JzWJh2BPlJjuI130_head
{
this:
np:hasAssertion
dgn-np:NP648123.RApxXth5RgTY7Eb9Y1cv7jSxPlREt8r5JzWJh2BPlJjuI130_assertion
;
np:hasProvenance
dgn-np:NP648123.RApxXth5RgTY7Eb9Y1cv7jSxPlREt8r5JzWJh2BPlJjuI130_provenance
;
np:hasPublicationInfo
dgn-np:NP648123.RApxXth5RgTY7Eb9Y1cv7jSxPlREt8r5JzWJh2BPlJjuI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP648123.RApxXth5RgTY7Eb9Y1cv7jSxPlREt8r5JzWJh2BPlJjuI130_assertion
a
np:Assertion
.
dgn-np:NP648123.RApxXth5RgTY7Eb9Y1cv7jSxPlREt8r5JzWJh2BPlJjuI130_provenance
a
np:Provenance
.
dgn-np:NP648123.RApxXth5RgTY7Eb9Y1cv7jSxPlREt8r5JzWJh2BPlJjuI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP648123.RApxXth5RgTY7Eb9Y1cv7jSxPlREt8r5JzWJh2BPlJjuI130_assertion
{
miriam-gene:2720
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGN57ed61c7a0ef81ead7a1bcd6bd70bd9f
sio:SIO_000628
miriam-gene:2720
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP648123.RApxXth5RgTY7Eb9Y1cv7jSxPlREt8r5JzWJh2BPlJjuI130_provenance
{
dgn-np:NP648123.RApxXth5RgTY7Eb9Y1cv7jSxPlREt8r5JzWJh2BPlJjuI130_assertion
dcterms:description
"[To determine whether C/EBP-epsilon behaves as an altered tumor-suppressor gene, samples from patients with acute myelogenous leukemia (AML) and myelodysplastic syndrome (MDS) evolving to AML were studied for loss of heterozygosity (LOH) using microsatellite sequences that we identified within 0.2 kb of the amino-terminus of the human C/EBP-epsilon gene.]. 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:9393598
;
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:NP648123.RApxXth5RgTY7Eb9Y1cv7jSxPlREt8r5JzWJh2BPlJjuI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:30+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" .
}