@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP568428.RABAII7iN_va_Nr5m3LAADeRPL65dnC_RfK01CHfHAtfQ
> .
@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:NP568428.RABAII7iN_va_Nr5m3LAADeRPL65dnC_RfK01CHfHAtfQ130_head
{
this:
np:hasAssertion
dgn-np:NP568428.RABAII7iN_va_Nr5m3LAADeRPL65dnC_RfK01CHfHAtfQ130_assertion
;
np:hasProvenance
dgn-np:NP568428.RABAII7iN_va_Nr5m3LAADeRPL65dnC_RfK01CHfHAtfQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP568428.RABAII7iN_va_Nr5m3LAADeRPL65dnC_RfK01CHfHAtfQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP568428.RABAII7iN_va_Nr5m3LAADeRPL65dnC_RfK01CHfHAtfQ130_assertion
a
np:Assertion
.
dgn-np:NP568428.RABAII7iN_va_Nr5m3LAADeRPL65dnC_RfK01CHfHAtfQ130_provenance
a
np:Provenance
.
dgn-np:NP568428.RABAII7iN_va_Nr5m3LAADeRPL65dnC_RfK01CHfHAtfQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP568428.RABAII7iN_va_Nr5m3LAADeRPL65dnC_RfK01CHfHAtfQ130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0017638
a
ncit:C7057
.
dgn-gda:DGN73cbadf95f0d2e24acc2fde99df3337e
sio:SIO_000628
miriam-gene:3342
,
lld:C0017638
;
a
sio:SIO_001121
.
}
dgn-np:NP568428.RABAII7iN_va_Nr5m3LAADeRPL65dnC_RfK01CHfHAtfQ130_provenance
{
dgn-np:NP568428.RABAII7iN_va_Nr5m3LAADeRPL65dnC_RfK01CHfHAtfQ130_assertion
dcterms:description
"[We investigated 23 pediatric nonependymal, nonpilocytic gliomas for chromosomal copy number aberrations (CNAs) by comparative genomic hybridization (CGH), mutations of isocitrate dehydrogenase (IDH) genes by direct sequencing, and proliferative activity and expression of O-methylguanine-DNA methyltransferase (MGMT) by immunohistochemistry.]. 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:21099717
;
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:NP568428.RABAII7iN_va_Nr5m3LAADeRPL65dnC_RfK01CHfHAtfQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:43+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" .
}