@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP268985.RAb0pbCntO9e6huxnlfk2_i5FieRvc2MfvOqZu_y8LG_w
> .
@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:NP268985.RAb0pbCntO9e6huxnlfk2_i5FieRvc2MfvOqZu_y8LG_w130_head
{
this:
np:hasAssertion
dgn-np:NP268985.RAb0pbCntO9e6huxnlfk2_i5FieRvc2MfvOqZu_y8LG_w130_assertion
;
np:hasProvenance
dgn-np:NP268985.RAb0pbCntO9e6huxnlfk2_i5FieRvc2MfvOqZu_y8LG_w130_provenance
;
np:hasPublicationInfo
dgn-np:NP268985.RAb0pbCntO9e6huxnlfk2_i5FieRvc2MfvOqZu_y8LG_w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP268985.RAb0pbCntO9e6huxnlfk2_i5FieRvc2MfvOqZu_y8LG_w130_assertion
a
np:Assertion
.
dgn-np:NP268985.RAb0pbCntO9e6huxnlfk2_i5FieRvc2MfvOqZu_y8LG_w130_provenance
a
np:Provenance
.
dgn-np:NP268985.RAb0pbCntO9e6huxnlfk2_i5FieRvc2MfvOqZu_y8LG_w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP268985.RAb0pbCntO9e6huxnlfk2_i5FieRvc2MfvOqZu_y8LG_w130_assertion
{
miriam-gene:10215
a
ncit:C16612
.
lld:C0014474
a
ncit:C7057
.
dgn-gda:DGN233c154fc4fbd97843ecea0490c8fa0b
sio:SIO_000628
miriam-gene:10215
,
lld:C0014474
;
a
sio:SIO_001121
.
}
dgn-np:NP268985.RAb0pbCntO9e6huxnlfk2_i5FieRvc2MfvOqZu_y8LG_w130_provenance
{
dgn-np:NP268985.RAb0pbCntO9e6huxnlfk2_i5FieRvc2MfvOqZu_y8LG_w130_assertion
dcterms:description
"[In contrast to the various types of pediatric astrocytic tumors, all ependymomas WHO grade II, regardless of site of origin, showed at most minimal OLIG2 expression, suggesting that OLIG2 function in pediatric gliomas is cell lineage dependent.]. 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:21193945
;
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:NP268985.RAb0pbCntO9e6huxnlfk2_i5FieRvc2MfvOqZu_y8LG_w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:30+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" .
}