@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP235094.RAd5t0z7y36E-d8wSyrEBog1UB5RY_k3Rh2RzV7NOw7aQ
> .
@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:NP235094.RAd5t0z7y36E-d8wSyrEBog1UB5RY_k3Rh2RzV7NOw7aQ130_head
{
this:
np:hasAssertion
dgn-np:NP235094.RAd5t0z7y36E-d8wSyrEBog1UB5RY_k3Rh2RzV7NOw7aQ130_assertion
;
np:hasProvenance
dgn-np:NP235094.RAd5t0z7y36E-d8wSyrEBog1UB5RY_k3Rh2RzV7NOw7aQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP235094.RAd5t0z7y36E-d8wSyrEBog1UB5RY_k3Rh2RzV7NOw7aQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP235094.RAd5t0z7y36E-d8wSyrEBog1UB5RY_k3Rh2RzV7NOw7aQ130_assertion
a
np:Assertion
.
dgn-np:NP235094.RAd5t0z7y36E-d8wSyrEBog1UB5RY_k3Rh2RzV7NOw7aQ130_provenance
a
np:Provenance
.
dgn-np:NP235094.RAd5t0z7y36E-d8wSyrEBog1UB5RY_k3Rh2RzV7NOw7aQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP235094.RAd5t0z7y36E-d8wSyrEBog1UB5RY_k3Rh2RzV7NOw7aQ130_assertion
{
miriam-gene:7248
a
ncit:C16612
.
lld:C1300127
a
ncit:C7057
.
dgn-gda:DGN3b25ae48b2f72241e133527048d6f5e8
sio:SIO_000628
miriam-gene:7248
,
lld:C1300127
;
a
sio:SIO_001121
.
}
dgn-np:NP235094.RAd5t0z7y36E-d8wSyrEBog1UB5RY_k3Rh2RzV7NOw7aQ130_provenance
{
dgn-np:NP235094.RAd5t0z7y36E-d8wSyrEBog1UB5RY_k3Rh2RzV7NOw7aQ130_assertion
dcterms:description
"[PEComas are related to the genetic alterations of tuberous sclerosis complex (TSC), an autosomal dominant genetic disease due to losses of TSC1 (9q34) or TSC2 (16p13.3) genes which seem to have a role in the regulation of the Rheb/mTOR/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:18080139
;
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:NP235094.RAd5t0z7y36E-d8wSyrEBog1UB5RY_k3Rh2RzV7NOw7aQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:12+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" .
}