@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP241010.RAEe7_RnnpCEHLoKMbrsQ7TV3R9eGKrUTcesJstpqteK4
> .
@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:NP241010.RAEe7_RnnpCEHLoKMbrsQ7TV3R9eGKrUTcesJstpqteK4130_head
{
this:
np:hasAssertion
dgn-np:NP241010.RAEe7_RnnpCEHLoKMbrsQ7TV3R9eGKrUTcesJstpqteK4130_assertion
;
np:hasProvenance
dgn-np:NP241010.RAEe7_RnnpCEHLoKMbrsQ7TV3R9eGKrUTcesJstpqteK4130_provenance
;
np:hasPublicationInfo
dgn-np:NP241010.RAEe7_RnnpCEHLoKMbrsQ7TV3R9eGKrUTcesJstpqteK4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP241010.RAEe7_RnnpCEHLoKMbrsQ7TV3R9eGKrUTcesJstpqteK4130_assertion
a
np:Assertion
.
dgn-np:NP241010.RAEe7_RnnpCEHLoKMbrsQ7TV3R9eGKrUTcesJstpqteK4130_provenance
a
np:Provenance
.
dgn-np:NP241010.RAEe7_RnnpCEHLoKMbrsQ7TV3R9eGKrUTcesJstpqteK4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP241010.RAEe7_RnnpCEHLoKMbrsQ7TV3R9eGKrUTcesJstpqteK4130_assertion
{
miriam-gene:4790
a
ncit:C16612
.
lld:C0017638
a
ncit:C7057
.
dgn-gda:DGN06976fc6e8f699a53ff8ee1441be43f1
sio:SIO_000628
miriam-gene:4790
,
lld:C0017638
;
a
sio:SIO_001121
.
}
dgn-np:NP241010.RAEe7_RnnpCEHLoKMbrsQ7TV3R9eGKrUTcesJstpqteK4130_provenance
{
dgn-np:NP241010.RAEe7_RnnpCEHLoKMbrsQ7TV3R9eGKrUTcesJstpqteK4130_assertion
dcterms:description
"[Gene expression profiling also identified components of the Notch pathway as being deregulated in glioma CSCs, and the deregulated expression of these genes was sensitive to treatment with STAT3 and NF-κB inhibitors.]. 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:23902772
;
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:NP241010.RAEe7_RnnpCEHLoKMbrsQ7TV3R9eGKrUTcesJstpqteK4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:15+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" .
}