@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP678850.RANfTmo0VEydBYda9lFAIF0NwuyctrTnqb9Ehz-lbejKI
> .
@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:NP678850.RANfTmo0VEydBYda9lFAIF0NwuyctrTnqb9Ehz-lbejKI130_head
{
this:
np:hasAssertion
dgn-np:NP678850.RANfTmo0VEydBYda9lFAIF0NwuyctrTnqb9Ehz-lbejKI130_assertion
;
np:hasProvenance
dgn-np:NP678850.RANfTmo0VEydBYda9lFAIF0NwuyctrTnqb9Ehz-lbejKI130_provenance
;
np:hasPublicationInfo
dgn-np:NP678850.RANfTmo0VEydBYda9lFAIF0NwuyctrTnqb9Ehz-lbejKI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP678850.RANfTmo0VEydBYda9lFAIF0NwuyctrTnqb9Ehz-lbejKI130_assertion
a
np:Assertion
.
dgn-np:NP678850.RANfTmo0VEydBYda9lFAIF0NwuyctrTnqb9Ehz-lbejKI130_provenance
a
np:Provenance
.
dgn-np:NP678850.RANfTmo0VEydBYda9lFAIF0NwuyctrTnqb9Ehz-lbejKI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP678850.RANfTmo0VEydBYda9lFAIF0NwuyctrTnqb9Ehz-lbejKI130_assertion
{
miriam-gene:2475
a
ncit:C16612
.
lld:C0524620
a
ncit:C7057
.
dgn-gda:DGNe11b3e41d26807f38c2f5c4428608721
sio:SIO_000628
miriam-gene:2475
,
lld:C0524620
;
a
sio:SIO_001121
.
}
dgn-np:NP678850.RANfTmo0VEydBYda9lFAIF0NwuyctrTnqb9Ehz-lbejKI130_provenance
{
dgn-np:NP678850.RANfTmo0VEydBYda9lFAIF0NwuyctrTnqb9Ehz-lbejKI130_assertion
dcterms:description
"[Experiments with overactivation or disruption of key lifespan determinant pathways, such as silent information regulator (SIR)T1, p66Shc, and mammalian target of rapamycin (TOR), lead to development of features of the metabolic syndrome in mice.]. 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:21040402
;
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:NP678850.RANfTmo0VEydBYda9lFAIF0NwuyctrTnqb9Ehz-lbejKI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:49+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" .
}