@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP592901.RAfqhXxZffj2Mg5gU1W8WBTfWqBSrPSG5Q4SDMLmUnFWA
> .
@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:NP592901.RAfqhXxZffj2Mg5gU1W8WBTfWqBSrPSG5Q4SDMLmUnFWA130_head
{
this:
np:hasAssertion
dgn-np:NP592901.RAfqhXxZffj2Mg5gU1W8WBTfWqBSrPSG5Q4SDMLmUnFWA130_assertion
;
np:hasProvenance
dgn-np:NP592901.RAfqhXxZffj2Mg5gU1W8WBTfWqBSrPSG5Q4SDMLmUnFWA130_provenance
;
np:hasPublicationInfo
dgn-np:NP592901.RAfqhXxZffj2Mg5gU1W8WBTfWqBSrPSG5Q4SDMLmUnFWA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP592901.RAfqhXxZffj2Mg5gU1W8WBTfWqBSrPSG5Q4SDMLmUnFWA130_assertion
a
np:Assertion
.
dgn-np:NP592901.RAfqhXxZffj2Mg5gU1W8WBTfWqBSrPSG5Q4SDMLmUnFWA130_provenance
a
np:Provenance
.
dgn-np:NP592901.RAfqhXxZffj2Mg5gU1W8WBTfWqBSrPSG5Q4SDMLmUnFWA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP592901.RAfqhXxZffj2Mg5gU1W8WBTfWqBSrPSG5Q4SDMLmUnFWA130_assertion
{
miriam-gene:6774
a
ncit:C16612
.
lld:C1457883
a
ncit:C7057
.
dgn-gda:DGN7432eb603076b851b7b992b752909af9
sio:SIO_000628
miriam-gene:6774
,
lld:C1457883
;
a
sio:SIO_001121
.
}
dgn-np:NP592901.RAfqhXxZffj2Mg5gU1W8WBTfWqBSrPSG5Q4SDMLmUnFWA130_provenance
{
dgn-np:NP592901.RAfqhXxZffj2Mg5gU1W8WBTfWqBSrPSG5Q4SDMLmUnFWA130_assertion
dcterms:description
"[Ectopic co-expression of C/EBPbeta and STAT3 reprograms neural stem cells along the aberrant mesenchymal lineage, whereas elimination of the two factors in glioma cells leads to collapse of the mesenchymal signature and reduces tumour aggressiveness.]. 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:20032975
;
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:NP592901.RAfqhXxZffj2Mg5gU1W8WBTfWqBSrPSG5Q4SDMLmUnFWA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:56+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" .
}