@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP870636.RAIxesehgH_Tx5LFkMHuDP0pq8NiA2IExCBMzUxprc13o
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP870636.RAIxesehgH_Tx5LFkMHuDP0pq8NiA2IExCBMzUxprc13o130_assertion
;
np:hasProvenance
dgn-np:NP870636.RAIxesehgH_Tx5LFkMHuDP0pq8NiA2IExCBMzUxprc13o130_provenance
;
np:hasPublicationInfo
dgn-np:NP870636.RAIxesehgH_Tx5LFkMHuDP0pq8NiA2IExCBMzUxprc13o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP870636.RAIxesehgH_Tx5LFkMHuDP0pq8NiA2IExCBMzUxprc13o130_assertion
a
np:Assertion
.
dgn-np:NP870636.RAIxesehgH_Tx5LFkMHuDP0pq8NiA2IExCBMzUxprc13o130_provenance
a
np:Provenance
.
dgn-np:NP870636.RAIxesehgH_Tx5LFkMHuDP0pq8NiA2IExCBMzUxprc13o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP870636.RAIxesehgH_Tx5LFkMHuDP0pq8NiA2IExCBMzUxprc13o130_assertion
{
miriam-gene:6662
a
ncit:C16612
.
lld:C0006118
a
ncit:C7057
.
dgn-gda:DGN3efdd28069a2163877884956d94a39bb
sio:SIO_000628
miriam-gene:6662
,
lld:C0006118
;
a
sio:SIO_001121
.
}
dgn-np:NP870636.RAIxesehgH_Tx5LFkMHuDP0pq8NiA2IExCBMzUxprc13o130_provenance
{
dgn-np:NP870636.RAIxesehgH_Tx5LFkMHuDP0pq8NiA2IExCBMzUxprc13o130_assertion
dcterms:description
"[Furthermore, our findings support further analysis of the functional properties of the selected genes, especially SOX4 and BCAT1 for medulloblastoma and SOX9 for ependymoma, to evaluate the use of these genes as potential tumor markers, prognostic markers, and drug targets in pediatric brain tumors.]. 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:18577562
;
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 .
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dgn-np:NP870636.RAIxesehgH_Tx5LFkMHuDP0pq8NiA2IExCBMzUxprc13o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:52+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" .
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"v2.1.0" .
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