@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP295616.RAytIkliqYSakA22VsB5FqlruF4P78OGaU8lyOWphRBas
> .
@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:NP295616.RAytIkliqYSakA22VsB5FqlruF4P78OGaU8lyOWphRBas130_head
{
this:
np:hasAssertion
dgn-np:NP295616.RAytIkliqYSakA22VsB5FqlruF4P78OGaU8lyOWphRBas130_assertion
;
np:hasProvenance
dgn-np:NP295616.RAytIkliqYSakA22VsB5FqlruF4P78OGaU8lyOWphRBas130_provenance
;
np:hasPublicationInfo
dgn-np:NP295616.RAytIkliqYSakA22VsB5FqlruF4P78OGaU8lyOWphRBas130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP295616.RAytIkliqYSakA22VsB5FqlruF4P78OGaU8lyOWphRBas130_assertion
a
np:Assertion
.
dgn-np:NP295616.RAytIkliqYSakA22VsB5FqlruF4P78OGaU8lyOWphRBas130_provenance
a
np:Provenance
.
dgn-np:NP295616.RAytIkliqYSakA22VsB5FqlruF4P78OGaU8lyOWphRBas130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP295616.RAytIkliqYSakA22VsB5FqlruF4P78OGaU8lyOWphRBas130_assertion
{
miriam-gene:4609
a
ncit:C16612
.
lld:C0376358
a
ncit:C7057
.
dgn-gda:DGNbe437b6308e5a4424daf3ac0f6e1006a
sio:SIO_000628
miriam-gene:4609
,
lld:C0376358
;
a
sio:SIO_001121
.
}
dgn-np:NP295616.RAytIkliqYSakA22VsB5FqlruF4P78OGaU8lyOWphRBas130_provenance
{
dgn-np:NP295616.RAytIkliqYSakA22VsB5FqlruF4P78OGaU8lyOWphRBas130_assertion
dcterms:description
"[In both normal and malignant prostate tissues, FOXP3 is both necessary and sufficient to transcriptionally repress cMYC, the most commonly overexpressed oncogene in prostate cancer as well as among the aggregates of other cancers.]. 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:19800578
;
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:NP295616.RAytIkliqYSakA22VsB5FqlruF4P78OGaU8lyOWphRBas130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:48+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" .
}