@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP513472.RA2kwMMbp-Ca2P96wqjbUVm2XQmLpqIdHuSd3rP_4fq4g
> .
@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:NP513472.RA2kwMMbp-Ca2P96wqjbUVm2XQmLpqIdHuSd3rP_4fq4g130_head
{
this:
np:hasAssertion
dgn-np:NP513472.RA2kwMMbp-Ca2P96wqjbUVm2XQmLpqIdHuSd3rP_4fq4g130_assertion
;
np:hasProvenance
dgn-np:NP513472.RA2kwMMbp-Ca2P96wqjbUVm2XQmLpqIdHuSd3rP_4fq4g130_provenance
;
np:hasPublicationInfo
dgn-np:NP513472.RA2kwMMbp-Ca2P96wqjbUVm2XQmLpqIdHuSd3rP_4fq4g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP513472.RA2kwMMbp-Ca2P96wqjbUVm2XQmLpqIdHuSd3rP_4fq4g130_assertion
a
np:Assertion
.
dgn-np:NP513472.RA2kwMMbp-Ca2P96wqjbUVm2XQmLpqIdHuSd3rP_4fq4g130_provenance
a
np:Provenance
.
dgn-np:NP513472.RA2kwMMbp-Ca2P96wqjbUVm2XQmLpqIdHuSd3rP_4fq4g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP513472.RA2kwMMbp-Ca2P96wqjbUVm2XQmLpqIdHuSd3rP_4fq4g130_assertion
{
miriam-gene:7249
a
ncit:C16612
.
lld:C0027765
a
ncit:C7057
.
dgn-gda:DGN8e1a4a842a81ecc1ff34db7c4740a562
sio:SIO_000628
miriam-gene:7249
,
lld:C0027765
;
a
sio:SIO_001121
.
}
dgn-np:NP513472.RA2kwMMbp-Ca2P96wqjbUVm2XQmLpqIdHuSd3rP_4fq4g130_provenance
{
dgn-np:NP513472.RA2kwMMbp-Ca2P96wqjbUVm2XQmLpqIdHuSd3rP_4fq4g130_assertion
dcterms:description
"[Loss of the tuberous sclerosis complex genes (TSC1 or TSC2) leads to constitutive activation of mTOR and downstream signaling elements, resulting in the development of tumors, neurological disorders, and at the cellular level, severe insulin/IGF-1 resistance.]. 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:18342602
;
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:NP513472.RA2kwMMbp-Ca2P96wqjbUVm2XQmLpqIdHuSd3rP_4fq4g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:06+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" .
}