@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP786796.RAkVoyiG1xdG9JO9JUnuYksxsYXd6nGfBfgTopcOJyBYI
> .
@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:NP786796.RAkVoyiG1xdG9JO9JUnuYksxsYXd6nGfBfgTopcOJyBYI130_head
{
this:
np:hasAssertion
dgn-np:NP786796.RAkVoyiG1xdG9JO9JUnuYksxsYXd6nGfBfgTopcOJyBYI130_assertion
;
np:hasProvenance
dgn-np:NP786796.RAkVoyiG1xdG9JO9JUnuYksxsYXd6nGfBfgTopcOJyBYI130_provenance
;
np:hasPublicationInfo
dgn-np:NP786796.RAkVoyiG1xdG9JO9JUnuYksxsYXd6nGfBfgTopcOJyBYI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP786796.RAkVoyiG1xdG9JO9JUnuYksxsYXd6nGfBfgTopcOJyBYI130_assertion
a
np:Assertion
.
dgn-np:NP786796.RAkVoyiG1xdG9JO9JUnuYksxsYXd6nGfBfgTopcOJyBYI130_provenance
a
np:Provenance
.
dgn-np:NP786796.RAkVoyiG1xdG9JO9JUnuYksxsYXd6nGfBfgTopcOJyBYI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP786796.RAkVoyiG1xdG9JO9JUnuYksxsYXd6nGfBfgTopcOJyBYI130_assertion
{
miriam-gene:8842
a
ncit:C16612
.
lld:C0014474
a
ncit:C7057
.
dgn-gda:DGN76e85413ffafd01903bbe58e8b5995a2
sio:SIO_000628
miriam-gene:8842
,
lld:C0014474
;
a
sio:SIO_001121
.
}
dgn-np:NP786796.RAkVoyiG1xdG9JO9JUnuYksxsYXd6nGfBfgTopcOJyBYI130_provenance
{
dgn-np:NP786796.RAkVoyiG1xdG9JO9JUnuYksxsYXd6nGfBfgTopcOJyBYI130_assertion
dcterms:description
"[The xenograft tumors shared nearly identical histopathological features with the original tumors, harbored 8 structural chromosomal abnormalities as detected with spectral karyotyping, maintained gene expression profiles resembling that of the original patient tumor with the preservation of multiple key genetic abnormalities commonly found in human ependymomas, and contained a small population (<2.2%) of CD133(+) stem cells that can form neurospheres and display multipotent capabilities in vitro.]. 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:20511191
;
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:NP786796.RAkVoyiG1xdG9JO9JUnuYksxsYXd6nGfBfgTopcOJyBYI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:00+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" .
}