@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP599148.RAYddQMnC7KcMXqFBIFfSpxjTx-FiaVgHZ73Uyj7tV150
> .
@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:NP599148.RAYddQMnC7KcMXqFBIFfSpxjTx-FiaVgHZ73Uyj7tV150130_head
{
this:
np:hasAssertion
dgn-np:NP599148.RAYddQMnC7KcMXqFBIFfSpxjTx-FiaVgHZ73Uyj7tV150130_assertion
;
np:hasProvenance
dgn-np:NP599148.RAYddQMnC7KcMXqFBIFfSpxjTx-FiaVgHZ73Uyj7tV150130_provenance
;
np:hasPublicationInfo
dgn-np:NP599148.RAYddQMnC7KcMXqFBIFfSpxjTx-FiaVgHZ73Uyj7tV150130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP599148.RAYddQMnC7KcMXqFBIFfSpxjTx-FiaVgHZ73Uyj7tV150130_assertion
a
np:Assertion
.
dgn-np:NP599148.RAYddQMnC7KcMXqFBIFfSpxjTx-FiaVgHZ73Uyj7tV150130_provenance
a
np:Provenance
.
dgn-np:NP599148.RAYddQMnC7KcMXqFBIFfSpxjTx-FiaVgHZ73Uyj7tV150130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP599148.RAYddQMnC7KcMXqFBIFfSpxjTx-FiaVgHZ73Uyj7tV150130_assertion
{
miriam-gene:6319
a
ncit:C16612
.
lld:C0027627
a
ncit:C7057
.
dgn-gda:DGNcf77a11c3d4e7b0db1af2e4a4316e269
sio:SIO_000628
miriam-gene:6319
,
lld:C0027627
;
a
sio:SIO_001121
.
}
dgn-np:NP599148.RAYddQMnC7KcMXqFBIFfSpxjTx-FiaVgHZ73Uyj7tV150130_provenance
{
dgn-np:NP599148.RAYddQMnC7KcMXqFBIFfSpxjTx-FiaVgHZ73Uyj7tV150130_assertion
dcterms:description
"[Increased SCD1 expression supports ccRCC viability and therefore we propose it as a novel molecular target for therapy either independently or in combination with an mTOR inhibitor for patients whose disease cannot be remedied with surgical intervention, such as in cases of advanced or metastatic disease.]. 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:23633458
;
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:NP599148.RAYddQMnC7KcMXqFBIFfSpxjTx-FiaVgHZ73Uyj7tV150130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:00+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" .
}