@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP554606.RAYhmSqX8sVXdSory-u-hvJqVaeANJmhNd6DBVux-URLY
> .
@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:NP554606.RAYhmSqX8sVXdSory-u-hvJqVaeANJmhNd6DBVux-URLY130_head
{
this:
np:hasAssertion
dgn-np:NP554606.RAYhmSqX8sVXdSory-u-hvJqVaeANJmhNd6DBVux-URLY130_assertion
;
np:hasProvenance
dgn-np:NP554606.RAYhmSqX8sVXdSory-u-hvJqVaeANJmhNd6DBVux-URLY130_provenance
;
np:hasPublicationInfo
dgn-np:NP554606.RAYhmSqX8sVXdSory-u-hvJqVaeANJmhNd6DBVux-URLY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP554606.RAYhmSqX8sVXdSory-u-hvJqVaeANJmhNd6DBVux-URLY130_assertion
a
np:Assertion
.
dgn-np:NP554606.RAYhmSqX8sVXdSory-u-hvJqVaeANJmhNd6DBVux-URLY130_provenance
a
np:Provenance
.
dgn-np:NP554606.RAYhmSqX8sVXdSory-u-hvJqVaeANJmhNd6DBVux-URLY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP554606.RAYhmSqX8sVXdSory-u-hvJqVaeANJmhNd6DBVux-URLY130_assertion
{
miriam-gene:7405
a
ncit:C16612
.
lld:C0009402
a
ncit:C7057
.
dgn-gda:DGN395ef9f836fab75514f2928552e64338
sio:SIO_000628
miriam-gene:7405
,
lld:C0009402
;
a
sio:SIO_001121
.
}
dgn-np:NP554606.RAYhmSqX8sVXdSory-u-hvJqVaeANJmhNd6DBVux-URLY130_provenance
{
dgn-np:NP554606.RAYhmSqX8sVXdSory-u-hvJqVaeANJmhNd6DBVux-URLY130_assertion
dcterms:description
"[In order to investigate whether the high incidence of UVRAG mutation in MSI colorectal carcinomas is associated with dysfunctional autophagy we analyzed autophagy levels in several colon cancer cell lines that express wild-type or mutant UVRAG protein.]. 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:20724836
;
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:NP554606.RAYhmSqX8sVXdSory-u-hvJqVaeANJmhNd6DBVux-URLY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:34+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" .
}