@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP773891.RAJSqtseQE0pedxE6gmjfcaBcErv-VzGw1r0h86tbUV5s
> .
@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:NP773891.RAJSqtseQE0pedxE6gmjfcaBcErv-VzGw1r0h86tbUV5s130_head
{
this:
np:hasAssertion
dgn-np:NP773891.RAJSqtseQE0pedxE6gmjfcaBcErv-VzGw1r0h86tbUV5s130_assertion
;
np:hasProvenance
dgn-np:NP773891.RAJSqtseQE0pedxE6gmjfcaBcErv-VzGw1r0h86tbUV5s130_provenance
;
np:hasPublicationInfo
dgn-np:NP773891.RAJSqtseQE0pedxE6gmjfcaBcErv-VzGw1r0h86tbUV5s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP773891.RAJSqtseQE0pedxE6gmjfcaBcErv-VzGw1r0h86tbUV5s130_assertion
a
np:Assertion
.
dgn-np:NP773891.RAJSqtseQE0pedxE6gmjfcaBcErv-VzGw1r0h86tbUV5s130_provenance
a
np:Provenance
.
dgn-np:NP773891.RAJSqtseQE0pedxE6gmjfcaBcErv-VzGw1r0h86tbUV5s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP773891.RAJSqtseQE0pedxE6gmjfcaBcErv-VzGw1r0h86tbUV5s130_assertion
{
miriam-gene:7249
a
ncit:C16612
.
lld:C0019247
a
ncit:C7057
.
dgn-gda:DGN2e038326f6b939391ba3c5d673a11074
sio:SIO_000628
miriam-gene:7249
,
lld:C0019247
;
a
sio:SIO_001121
.
}
dgn-np:NP773891.RAJSqtseQE0pedxE6gmjfcaBcErv-VzGw1r0h86tbUV5s130_provenance
{
dgn-np:NP773891.RAJSqtseQE0pedxE6gmjfcaBcErv-VzGw1r0h86tbUV5s130_assertion
dcterms:description
"[Striking improvements in the understanding of the genetic basis of this autosomal dominant genetic disease are coupled to the understanding of the mechanisms that link the loss of TSC1 (9q34) or TSC2 (16p13.3) genes with the regulation of the Rheb/m-TOR/p70S6K pathway.]. 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:20073603
;
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:NP773891.RAJSqtseQE0pedxE6gmjfcaBcErv-VzGw1r0h86tbUV5s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:48+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" .
}