@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP873999.RAL8zKMyaYaBB-YcAsLydnqeJlII4ouv8x0uJVH_j4TFw
> .
@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:NP873999.RAL8zKMyaYaBB-YcAsLydnqeJlII4ouv8x0uJVH_j4TFw130_head
{
this:
np:hasAssertion
dgn-np:NP873999.RAL8zKMyaYaBB-YcAsLydnqeJlII4ouv8x0uJVH_j4TFw130_assertion
;
np:hasProvenance
dgn-np:NP873999.RAL8zKMyaYaBB-YcAsLydnqeJlII4ouv8x0uJVH_j4TFw130_provenance
;
np:hasPublicationInfo
dgn-np:NP873999.RAL8zKMyaYaBB-YcAsLydnqeJlII4ouv8x0uJVH_j4TFw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP873999.RAL8zKMyaYaBB-YcAsLydnqeJlII4ouv8x0uJVH_j4TFw130_assertion
a
np:Assertion
.
dgn-np:NP873999.RAL8zKMyaYaBB-YcAsLydnqeJlII4ouv8x0uJVH_j4TFw130_provenance
a
np:Provenance
.
dgn-np:NP873999.RAL8zKMyaYaBB-YcAsLydnqeJlII4ouv8x0uJVH_j4TFw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP873999.RAL8zKMyaYaBB-YcAsLydnqeJlII4ouv8x0uJVH_j4TFw130_assertion
{
miriam-gene:6659
a
ncit:C16612
.
lld:C0006118
a
ncit:C7057
.
dgn-gda:DGNb60b2717a35cb8e5bf051e6402245d06
sio:SIO_000628
miriam-gene:6659
,
lld:C0006118
;
a
sio:SIO_001121
.
}
dgn-np:NP873999.RAL8zKMyaYaBB-YcAsLydnqeJlII4ouv8x0uJVH_j4TFw130_provenance
{
dgn-np:NP873999.RAL8zKMyaYaBB-YcAsLydnqeJlII4ouv8x0uJVH_j4TFw130_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 .
}
dgn-np:NP873999.RAL8zKMyaYaBB-YcAsLydnqeJlII4ouv8x0uJVH_j4TFw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:54+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" .
}