@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP367974.RAmC9wmT3boheMnJBMFJxRQwLhAJU9O_G25FgBq_ToY5g
> .
@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:NP367974.RAmC9wmT3boheMnJBMFJxRQwLhAJU9O_G25FgBq_ToY5g130_head
{
this:
np:hasAssertion
dgn-np:NP367974.RAmC9wmT3boheMnJBMFJxRQwLhAJU9O_G25FgBq_ToY5g130_assertion
;
np:hasProvenance
dgn-np:NP367974.RAmC9wmT3boheMnJBMFJxRQwLhAJU9O_G25FgBq_ToY5g130_provenance
;
np:hasPublicationInfo
dgn-np:NP367974.RAmC9wmT3boheMnJBMFJxRQwLhAJU9O_G25FgBq_ToY5g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP367974.RAmC9wmT3boheMnJBMFJxRQwLhAJU9O_G25FgBq_ToY5g130_assertion
a
np:Assertion
.
dgn-np:NP367974.RAmC9wmT3boheMnJBMFJxRQwLhAJU9O_G25FgBq_ToY5g130_provenance
a
np:Provenance
.
dgn-np:NP367974.RAmC9wmT3boheMnJBMFJxRQwLhAJU9O_G25FgBq_ToY5g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP367974.RAmC9wmT3boheMnJBMFJxRQwLhAJU9O_G25FgBq_ToY5g130_assertion
{
miriam-gene:6581
a
ncit:C16612
.
lld:C1621958
a
ncit:C7057
.
dgn-gda:DGN5b7ff33157c60a4f0e4d2dd6043ca0a8
sio:SIO_000628
miriam-gene:6581
,
lld:C1621958
;
a
sio:SIO_001121
.
}
dgn-np:NP367974.RAmC9wmT3boheMnJBMFJxRQwLhAJU9O_G25FgBq_ToY5g130_provenance
{
dgn-np:NP367974.RAmC9wmT3boheMnJBMFJxRQwLhAJU9O_G25FgBq_ToY5g130_assertion
dcterms: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:NP367974.RAmC9wmT3boheMnJBMFJxRQwLhAJU9O_G25FgBq_ToY5g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:35+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" .
}