@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP548619.RA3uJqwL47bsIXQhTBkHZNfGzWZIiQFu0KL5FIyGkOsig
> .
@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:NP548619.RA3uJqwL47bsIXQhTBkHZNfGzWZIiQFu0KL5FIyGkOsig130_head
{
this:
np:hasAssertion
dgn-np:NP548619.RA3uJqwL47bsIXQhTBkHZNfGzWZIiQFu0KL5FIyGkOsig130_assertion
;
np:hasProvenance
dgn-np:NP548619.RA3uJqwL47bsIXQhTBkHZNfGzWZIiQFu0KL5FIyGkOsig130_provenance
;
np:hasPublicationInfo
dgn-np:NP548619.RA3uJqwL47bsIXQhTBkHZNfGzWZIiQFu0KL5FIyGkOsig130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP548619.RA3uJqwL47bsIXQhTBkHZNfGzWZIiQFu0KL5FIyGkOsig130_assertion
a
np:Assertion
.
dgn-np:NP548619.RA3uJqwL47bsIXQhTBkHZNfGzWZIiQFu0KL5FIyGkOsig130_provenance
a
np:Provenance
.
dgn-np:NP548619.RA3uJqwL47bsIXQhTBkHZNfGzWZIiQFu0KL5FIyGkOsig130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP548619.RA3uJqwL47bsIXQhTBkHZNfGzWZIiQFu0KL5FIyGkOsig130_assertion
{
miriam-gene:2309
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN7bf6b41b40bc759e5748bea1c4988dca
sio:SIO_000628
miriam-gene:2309
,
lld:C0006142
;
a
sio:SIO_001121
.
}
dgn-np:NP548619.RA3uJqwL47bsIXQhTBkHZNfGzWZIiQFu0KL5FIyGkOsig130_provenance
{
dgn-np:NP548619.RA3uJqwL47bsIXQhTBkHZNfGzWZIiQFu0KL5FIyGkOsig130_assertion
dcterms:description
"[As such, sustained nuclear FOXO3a expression in breast cancer may culminate in cancer progression and the development of an aggressive phenotype similar to that observed in cytotoxic chemotherapy resistant breast cancer cell models.]. 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:20808831
;
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:NP548619.RA3uJqwL47bsIXQhTBkHZNfGzWZIiQFu0KL5FIyGkOsig130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:30+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" .
}