@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP562052.RArqCY1oP78fBIANoZHNTm7Us4fihWDOwJ199HUoWWDKE
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP562052.RArqCY1oP78fBIANoZHNTm7Us4fihWDOwJ199HUoWWDKE130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP562052.RArqCY1oP78fBIANoZHNTm7Us4fihWDOwJ199HUoWWDKE130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP562052.RArqCY1oP78fBIANoZHNTm7Us4fihWDOwJ199HUoWWDKE130_assertion
a
np:Assertion
.
dgn-np:NP562052.RArqCY1oP78fBIANoZHNTm7Us4fihWDOwJ199HUoWWDKE130_provenance
a
np:Provenance
.
dgn-np:NP562052.RArqCY1oP78fBIANoZHNTm7Us4fihWDOwJ199HUoWWDKE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP562052.RArqCY1oP78fBIANoZHNTm7Us4fihWDOwJ199HUoWWDKE130_assertion
{
miriam-gene:596
a
ncit:C16612
.
lld:C0678222
a
ncit:C7057
.
dgn-gda:DGN55b7591cae1a4bfa9c0ab862f6cc6b71
sio:SIO_000628
miriam-gene:596
,
lld:C0678222
;
a
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.
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dgn-np:NP562052.RArqCY1oP78fBIANoZHNTm7Us4fihWDOwJ199HUoWWDKE130_provenance
{
dgn-np:NP562052.RArqCY1oP78fBIANoZHNTm7Us4fihWDOwJ199HUoWWDKE130_assertion
dcterms:description
"[shRNA mediated knock down of RHOXF1 can be effective in induction of apoptotic pathway in cancer cells via BCL2 downregulation, so it can have potential therapeutic utility for human breast 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:23317270
;
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 .
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dgn-np:NP562052.RArqCY1oP78fBIANoZHNTm7Us4fihWDOwJ199HUoWWDKE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:39+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
<
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> , <
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" .
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"v2.1.0" .
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