@prefix dc: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP368834.RACkmiqRZPIJW6kk2IKQBxV_DWNlfambuBbakbtms2-Qw
> .
@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 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:NP368834.RACkmiqRZPIJW6kk2IKQBxV_DWNlfambuBbakbtms2-Qw130_head
{
this:
np:hasAssertion
dgn-np:NP368834.RACkmiqRZPIJW6kk2IKQBxV_DWNlfambuBbakbtms2-Qw130_assertion
;
np:hasProvenance
dgn-np:NP368834.RACkmiqRZPIJW6kk2IKQBxV_DWNlfambuBbakbtms2-Qw130_provenance
;
np:hasPublicationInfo
dgn-np:NP368834.RACkmiqRZPIJW6kk2IKQBxV_DWNlfambuBbakbtms2-Qw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP368834.RACkmiqRZPIJW6kk2IKQBxV_DWNlfambuBbakbtms2-Qw130_assertion
a
np:Assertion
.
dgn-np:NP368834.RACkmiqRZPIJW6kk2IKQBxV_DWNlfambuBbakbtms2-Qw130_provenance
a
np:Provenance
.
dgn-np:NP368834.RACkmiqRZPIJW6kk2IKQBxV_DWNlfambuBbakbtms2-Qw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP368834.RACkmiqRZPIJW6kk2IKQBxV_DWNlfambuBbakbtms2-Qw130_assertion
{
miriam-gene:3702
a
ncit:C16612
.
lld:C0017636
a
ncit:C7057
.
dgn-gda:DGN24eeaa9c8ee4442284a2135466bf1b28
sio:SIO_000628
miriam-gene:3702
,
lld:C0017636
;
a
sio:SIO_001121
.
}
dgn-np:NP368834.RACkmiqRZPIJW6kk2IKQBxV_DWNlfambuBbakbtms2-Qw130_provenance
{
dgn-np:NP368834.RACkmiqRZPIJW6kk2IKQBxV_DWNlfambuBbakbtms2-Qw130_assertion
dc:description
"[While the mesenchymal subtype of GBM displays similarity with the signatures of both EMT and CD133, it also exhibits some differences with each of these signatures that are partly due to the fact that the signatures of EMT and CD133 are inversely related to each other.]. 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:23734191
;
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:NP368834.RACkmiqRZPIJW6kk2IKQBxV_DWNlfambuBbakbtms2-Qw130_publicationInfo
{
this:
dc:created
"2014-10-02T12:35:35+02:00"^^
xsd:dateTime
;
dc:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dc:rightsHolder
dgn-void:IBIGroup
;
dc: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" .
}