@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP201358.RAgp8WbKuu0ACNlWQHeZIM1wb9XPhOfGNoHp69vlrqmHE
> .
@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:NP201358.RAgp8WbKuu0ACNlWQHeZIM1wb9XPhOfGNoHp69vlrqmHE130_head
{
this:
np:hasAssertion
dgn-np:NP201358.RAgp8WbKuu0ACNlWQHeZIM1wb9XPhOfGNoHp69vlrqmHE130_assertion
;
np:hasProvenance
dgn-np:NP201358.RAgp8WbKuu0ACNlWQHeZIM1wb9XPhOfGNoHp69vlrqmHE130_provenance
;
np:hasPublicationInfo
dgn-np:NP201358.RAgp8WbKuu0ACNlWQHeZIM1wb9XPhOfGNoHp69vlrqmHE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP201358.RAgp8WbKuu0ACNlWQHeZIM1wb9XPhOfGNoHp69vlrqmHE130_assertion
a
np:Assertion
.
dgn-np:NP201358.RAgp8WbKuu0ACNlWQHeZIM1wb9XPhOfGNoHp69vlrqmHE130_provenance
a
np:Provenance
.
dgn-np:NP201358.RAgp8WbKuu0ACNlWQHeZIM1wb9XPhOfGNoHp69vlrqmHE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP201358.RAgp8WbKuu0ACNlWQHeZIM1wb9XPhOfGNoHp69vlrqmHE130_assertion
{
miriam-gene:5728
a
ncit:C16612
.
lld:C1621958
a
ncit:C7057
.
dgn-gda:DGN7a7c71fa2cd7b6e831e56b7d9c7f755d
sio:SIO_000628
miriam-gene:5728
,
lld:C1621958
;
a
sio:SIO_001121
.
}
dgn-np:NP201358.RAgp8WbKuu0ACNlWQHeZIM1wb9XPhOfGNoHp69vlrqmHE130_provenance
{
dgn-np:NP201358.RAgp8WbKuu0ACNlWQHeZIM1wb9XPhOfGNoHp69vlrqmHE130_assertion
dcterms:description
"[Hyperactivation of the phosphatidylinositol 3-kinase/Akt signaling through disruption of PTEN function is common in glioblastoma multiforme, and these genetic changes are predicted to enhance sensitivity to mammalian target of rapamycin (mTOR) inhibitors such as RAD001 (everolimus).]. 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:18559622
;
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:NP201358.RAgp8WbKuu0ACNlWQHeZIM1wb9XPhOfGNoHp69vlrqmHE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:51+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" .
}