@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP689982.RATTgPuwFnS8xMiiFdwCKxFY1s2t2khiCBT0ANhbgVbIY
> .
@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:NP689982.RATTgPuwFnS8xMiiFdwCKxFY1s2t2khiCBT0ANhbgVbIY130_head
{
this:
np:hasAssertion
dgn-np:NP689982.RATTgPuwFnS8xMiiFdwCKxFY1s2t2khiCBT0ANhbgVbIY130_assertion
;
np:hasProvenance
dgn-np:NP689982.RATTgPuwFnS8xMiiFdwCKxFY1s2t2khiCBT0ANhbgVbIY130_provenance
;
np:hasPublicationInfo
dgn-np:NP689982.RATTgPuwFnS8xMiiFdwCKxFY1s2t2khiCBT0ANhbgVbIY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP689982.RATTgPuwFnS8xMiiFdwCKxFY1s2t2khiCBT0ANhbgVbIY130_assertion
a
np:Assertion
.
dgn-np:NP689982.RATTgPuwFnS8xMiiFdwCKxFY1s2t2khiCBT0ANhbgVbIY130_provenance
a
np:Provenance
.
dgn-np:NP689982.RATTgPuwFnS8xMiiFdwCKxFY1s2t2khiCBT0ANhbgVbIY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP689982.RATTgPuwFnS8xMiiFdwCKxFY1s2t2khiCBT0ANhbgVbIY130_assertion
{
miriam-gene:2475
a
ncit:C16612
.
lld:C0019247
a
ncit:C7057
.
dgn-gda:DGNba1a60f476b476b7ec0699d266668ed9
sio:SIO_000628
miriam-gene:2475
,
lld:C0019247
;
a
sio:SIO_001121
.
}
dgn-np:NP689982.RATTgPuwFnS8xMiiFdwCKxFY1s2t2khiCBT0ANhbgVbIY130_provenance
{
dgn-np:NP689982.RATTgPuwFnS8xMiiFdwCKxFY1s2t2khiCBT0ANhbgVbIY130_assertion
dcterms:description
"[Hyperactivation of the mTOR pathway, leading to increased cell growth and proliferation, has been most convincingly shown to stimulate tumor growth in the brain and other organs in the genetic disorder, tuberous sclerosis complex (TSC).]. 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:23644232
;
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:NP689982.RATTgPuwFnS8xMiiFdwCKxFY1s2t2khiCBT0ANhbgVbIY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:59+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" .
}