@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP786483.RA77a0QUQ12B0Y1KTHclUqejv9rFkoJth3_R325vn461w
> .
@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:NP786483.RA77a0QUQ12B0Y1KTHclUqejv9rFkoJth3_R325vn461w130_head
{
this:
np:hasAssertion
dgn-np:NP786483.RA77a0QUQ12B0Y1KTHclUqejv9rFkoJth3_R325vn461w130_assertion
;
np:hasProvenance
dgn-np:NP786483.RA77a0QUQ12B0Y1KTHclUqejv9rFkoJth3_R325vn461w130_provenance
;
np:hasPublicationInfo
dgn-np:NP786483.RA77a0QUQ12B0Y1KTHclUqejv9rFkoJth3_R325vn461w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP786483.RA77a0QUQ12B0Y1KTHclUqejv9rFkoJth3_R325vn461w130_assertion
a
np:Assertion
.
dgn-np:NP786483.RA77a0QUQ12B0Y1KTHclUqejv9rFkoJth3_R325vn461w130_provenance
a
np:Provenance
.
dgn-np:NP786483.RA77a0QUQ12B0Y1KTHclUqejv9rFkoJth3_R325vn461w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP786483.RA77a0QUQ12B0Y1KTHclUqejv9rFkoJth3_R325vn461w130_assertion
{
miriam-gene:6319
a
ncit:C16612
.
lld:C2939420
a
ncit:C7057
.
dgn-gda:DGNb22a8bed96ab8637467d3d8d5f55d1ae
sio:SIO_000628
miriam-gene:6319
,
lld:C2939420
;
a
sio:SIO_001121
.
}
dgn-np:NP786483.RA77a0QUQ12B0Y1KTHclUqejv9rFkoJth3_R325vn461w130_provenance
{
dgn-np:NP786483.RA77a0QUQ12B0Y1KTHclUqejv9rFkoJth3_R325vn461w130_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:NP786483.RA77a0QUQ12B0Y1KTHclUqejv9rFkoJth3_R325vn461w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:56+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" .
}