@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP421221.RAg254RR8ZUnysNM0RFoXVsumGP8K6TVvtEeGklHZ8vGw
> .
@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:NP421221.RAg254RR8ZUnysNM0RFoXVsumGP8K6TVvtEeGklHZ8vGw130_head
{
this:
np:hasAssertion
dgn-np:NP421221.RAg254RR8ZUnysNM0RFoXVsumGP8K6TVvtEeGklHZ8vGw130_assertion
;
np:hasProvenance
dgn-np:NP421221.RAg254RR8ZUnysNM0RFoXVsumGP8K6TVvtEeGklHZ8vGw130_provenance
;
np:hasPublicationInfo
dgn-np:NP421221.RAg254RR8ZUnysNM0RFoXVsumGP8K6TVvtEeGklHZ8vGw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP421221.RAg254RR8ZUnysNM0RFoXVsumGP8K6TVvtEeGklHZ8vGw130_assertion
a
np:Assertion
.
dgn-np:NP421221.RAg254RR8ZUnysNM0RFoXVsumGP8K6TVvtEeGklHZ8vGw130_provenance
a
np:Provenance
.
dgn-np:NP421221.RAg254RR8ZUnysNM0RFoXVsumGP8K6TVvtEeGklHZ8vGw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP421221.RAg254RR8ZUnysNM0RFoXVsumGP8K6TVvtEeGklHZ8vGw130_assertion
{
miriam-gene:7248
a
ncit:C16612
.
lld:C0007134
a
ncit:C7057
.
dgn-gda:DGN558b73d29aa78fe7d595ab3f13eebd42
sio:SIO_000628
miriam-gene:7248
,
lld:C0007134
;
a
sio:SIO_001121
.
}
dgn-np:NP421221.RAg254RR8ZUnysNM0RFoXVsumGP8K6TVvtEeGklHZ8vGw130_provenance
{
dgn-np:NP421221.RAg254RR8ZUnysNM0RFoXVsumGP8K6TVvtEeGklHZ8vGw130_assertion
dcterms:description
"[Here, we will address the genetic, cellular and biochemical mechanisms that may contribute to the unusually broad spectrum of renal disease in cells with TSC1 or TSC2 mutations, and consider how the TSC signaling pathways may be linked to other renal diseases such as polycystic kidney disease and renal cell carcinoma.]. 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:15856327
;
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:NP421221.RAg254RR8ZUnysNM0RFoXVsumGP8K6TVvtEeGklHZ8vGw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:10+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" .
}