@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP594716.RAt0R0jY1NYS0R5hrOTXtHUP8lyaXUoph6VY4UulI09bg
> .
@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:NP594716.RAt0R0jY1NYS0R5hrOTXtHUP8lyaXUoph6VY4UulI09bg130_head
{
this:
np:hasAssertion
dgn-np:NP594716.RAt0R0jY1NYS0R5hrOTXtHUP8lyaXUoph6VY4UulI09bg130_assertion
;
np:hasProvenance
dgn-np:NP594716.RAt0R0jY1NYS0R5hrOTXtHUP8lyaXUoph6VY4UulI09bg130_provenance
;
np:hasPublicationInfo
dgn-np:NP594716.RAt0R0jY1NYS0R5hrOTXtHUP8lyaXUoph6VY4UulI09bg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP594716.RAt0R0jY1NYS0R5hrOTXtHUP8lyaXUoph6VY4UulI09bg130_assertion
a
np:Assertion
.
dgn-np:NP594716.RAt0R0jY1NYS0R5hrOTXtHUP8lyaXUoph6VY4UulI09bg130_provenance
a
np:Provenance
.
dgn-np:NP594716.RAt0R0jY1NYS0R5hrOTXtHUP8lyaXUoph6VY4UulI09bg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP594716.RAt0R0jY1NYS0R5hrOTXtHUP8lyaXUoph6VY4UulI09bg130_assertion
{
miriam-gene:1746
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGNd2d01f403bb223f6582f19c9645b543d
sio:SIO_000628
miriam-gene:1746
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP594716.RAt0R0jY1NYS0R5hrOTXtHUP8lyaXUoph6VY4UulI09bg130_provenance
{
dgn-np:NP594716.RAt0R0jY1NYS0R5hrOTXtHUP8lyaXUoph6VY4UulI09bg130_assertion
dcterms:description
"[Annotation of mRNA profiling data on GBM from The Cancer Genome Atlas and MD Anderson Cancer Center showed the proneural and neural subtypes highly correlated with low and high DLX2 expression, respectively.]. 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:23331016
;
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:NP594716.RAt0R0jY1NYS0R5hrOTXtHUP8lyaXUoph6VY4UulI09bg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:57+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" .
}