@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP353151.RAbqmF7cQ9slnU80G4lFQqioFwdNvm0npZEY37o8kTpIk
> .
@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:NP353151.RAbqmF7cQ9slnU80G4lFQqioFwdNvm0npZEY37o8kTpIk130_head
{
this:
np:hasAssertion
dgn-np:NP353151.RAbqmF7cQ9slnU80G4lFQqioFwdNvm0npZEY37o8kTpIk130_assertion
;
np:hasProvenance
dgn-np:NP353151.RAbqmF7cQ9slnU80G4lFQqioFwdNvm0npZEY37o8kTpIk130_provenance
;
np:hasPublicationInfo
dgn-np:NP353151.RAbqmF7cQ9slnU80G4lFQqioFwdNvm0npZEY37o8kTpIk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP353151.RAbqmF7cQ9slnU80G4lFQqioFwdNvm0npZEY37o8kTpIk130_assertion
a
np:Assertion
.
dgn-np:NP353151.RAbqmF7cQ9slnU80G4lFQqioFwdNvm0npZEY37o8kTpIk130_provenance
a
np:Provenance
.
dgn-np:NP353151.RAbqmF7cQ9slnU80G4lFQqioFwdNvm0npZEY37o8kTpIk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP353151.RAbqmF7cQ9slnU80G4lFQqioFwdNvm0npZEY37o8kTpIk130_assertion
{
miriam-gene:1052
a
ncit:C16612
.
lld:C0035335
a
ncit:C7057
.
dgn-gda:DGN19756763290807b1658115762cd16a90
sio:SIO_000628
miriam-gene:1052
,
lld:C0035335
;
a
sio:SIO_001121
.
}
dgn-np:NP353151.RAbqmF7cQ9slnU80G4lFQqioFwdNvm0npZEY37o8kTpIk130_provenance
{
dgn-np:NP353151.RAbqmF7cQ9slnU80G4lFQqioFwdNvm0npZEY37o8kTpIk130_assertion
dcterms:description
"[Furthermore, a consequence of HMDB-induced CEBPD expression was linked with E2F1 and retinoblastoma (RB), which discloses the scenario of CEBPD, E2F1, and RB bindings and transcriptional regulation on the promoters of proapoptotic genes, PPARG2 and GADD153.]. 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:20971808
;
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:NP353151.RAbqmF7cQ9slnU80G4lFQqioFwdNvm0npZEY37o8kTpIk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:27+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" .
}