@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP756164.RAbdSbKCBsbmi7lwocN6RoBYnLl3npPJ0yDEniQq5CP2k
> .
@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:NP756164.RAbdSbKCBsbmi7lwocN6RoBYnLl3npPJ0yDEniQq5CP2k130_head
{
this:
np:hasAssertion
dgn-np:NP756164.RAbdSbKCBsbmi7lwocN6RoBYnLl3npPJ0yDEniQq5CP2k130_assertion
;
np:hasProvenance
dgn-np:NP756164.RAbdSbKCBsbmi7lwocN6RoBYnLl3npPJ0yDEniQq5CP2k130_provenance
;
np:hasPublicationInfo
dgn-np:NP756164.RAbdSbKCBsbmi7lwocN6RoBYnLl3npPJ0yDEniQq5CP2k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP756164.RAbdSbKCBsbmi7lwocN6RoBYnLl3npPJ0yDEniQq5CP2k130_assertion
a
np:Assertion
.
dgn-np:NP756164.RAbdSbKCBsbmi7lwocN6RoBYnLl3npPJ0yDEniQq5CP2k130_provenance
a
np:Provenance
.
dgn-np:NP756164.RAbdSbKCBsbmi7lwocN6RoBYnLl3npPJ0yDEniQq5CP2k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP756164.RAbdSbKCBsbmi7lwocN6RoBYnLl3npPJ0yDEniQq5CP2k130_assertion
{
miriam-gene:50943
a
ncit:C16612
.
lld:C0600139
a
ncit:C7057
.
dgn-gda:DGN21a06b8191ff6e1b209e6038e81cee90
sio:SIO_000628
miriam-gene:50943
,
lld:C0600139
;
a
sio:SIO_001121
.
}
dgn-np:NP756164.RAbdSbKCBsbmi7lwocN6RoBYnLl3npPJ0yDEniQq5CP2k130_provenance
{
dgn-np:NP756164.RAbdSbKCBsbmi7lwocN6RoBYnLl3npPJ0yDEniQq5CP2k130_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:NP756164.RAbdSbKCBsbmi7lwocN6RoBYnLl3npPJ0yDEniQq5CP2k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:38+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" .
}