@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP190989.RAXa0L5UUZclZyoGkKkTeAJYbmArqcIuMJhdg3wBVkCE8
> .
@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:NP190989.RAXa0L5UUZclZyoGkKkTeAJYbmArqcIuMJhdg3wBVkCE8130_head
{
this:
np:hasAssertion
dgn-np:NP190989.RAXa0L5UUZclZyoGkKkTeAJYbmArqcIuMJhdg3wBVkCE8130_assertion
;
np:hasProvenance
dgn-np:NP190989.RAXa0L5UUZclZyoGkKkTeAJYbmArqcIuMJhdg3wBVkCE8130_provenance
;
np:hasPublicationInfo
dgn-np:NP190989.RAXa0L5UUZclZyoGkKkTeAJYbmArqcIuMJhdg3wBVkCE8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP190989.RAXa0L5UUZclZyoGkKkTeAJYbmArqcIuMJhdg3wBVkCE8130_assertion
a
np:Assertion
.
dgn-np:NP190989.RAXa0L5UUZclZyoGkKkTeAJYbmArqcIuMJhdg3wBVkCE8130_provenance
a
np:Provenance
.
dgn-np:NP190989.RAXa0L5UUZclZyoGkKkTeAJYbmArqcIuMJhdg3wBVkCE8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP190989.RAXa0L5UUZclZyoGkKkTeAJYbmArqcIuMJhdg3wBVkCE8130_assertion
{
miriam-gene:2335
a
ncit:C16612
.
lld:C0033578
a
ncit:C7057
.
dgn-gda:DGN3d367dd4bab9956862499b4af0c85e63
sio:SIO_000628
miriam-gene:2335
,
lld:C0033578
;
a
sio:SIO_001121
.
}
dgn-np:NP190989.RAXa0L5UUZclZyoGkKkTeAJYbmArqcIuMJhdg3wBVkCE8130_provenance
{
dgn-np:NP190989.RAXa0L5UUZclZyoGkKkTeAJYbmArqcIuMJhdg3wBVkCE8130_assertion
dcterms:description
"[It is suggested that these defects in the suppressor network allow for the unopposed induction of TGFbeta1 and fibronectin, which favor transformation and survival of prostate tumor epithelial cells, and explain the role of Egr1 in prostate cancer.]. 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:16138117
;
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:NP190989.RAXa0L5UUZclZyoGkKkTeAJYbmArqcIuMJhdg3wBVkCE8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:45+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" .
}