@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP886111.RAeQ8JRMF61sRm5OUJ2hi5MvD0vGa8cTFXE-JsPwfFqYw
> .
@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:NP886111.RAeQ8JRMF61sRm5OUJ2hi5MvD0vGa8cTFXE-JsPwfFqYw130_head
{
this:
np:hasAssertion
dgn-np:NP886111.RAeQ8JRMF61sRm5OUJ2hi5MvD0vGa8cTFXE-JsPwfFqYw130_assertion
;
np:hasProvenance
dgn-np:NP886111.RAeQ8JRMF61sRm5OUJ2hi5MvD0vGa8cTFXE-JsPwfFqYw130_provenance
;
np:hasPublicationInfo
dgn-np:NP886111.RAeQ8JRMF61sRm5OUJ2hi5MvD0vGa8cTFXE-JsPwfFqYw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP886111.RAeQ8JRMF61sRm5OUJ2hi5MvD0vGa8cTFXE-JsPwfFqYw130_assertion
a
np:Assertion
.
dgn-np:NP886111.RAeQ8JRMF61sRm5OUJ2hi5MvD0vGa8cTFXE-JsPwfFqYw130_provenance
a
np:Provenance
.
dgn-np:NP886111.RAeQ8JRMF61sRm5OUJ2hi5MvD0vGa8cTFXE-JsPwfFqYw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP886111.RAeQ8JRMF61sRm5OUJ2hi5MvD0vGa8cTFXE-JsPwfFqYw130_assertion
{
miriam-gene:1302
a
ncit:C16612
.
lld:C0011849
a
ncit:C7057
.
dgn-gda:DGNf86279bfa5b9fff27bd622c624d1babf
sio:SIO_000628
miriam-gene:1302
,
lld:C0011849
;
a
sio:SIO_001121
.
}
dgn-np:NP886111.RAeQ8JRMF61sRm5OUJ2hi5MvD0vGa8cTFXE-JsPwfFqYw130_provenance
{
dgn-np:NP886111.RAeQ8JRMF61sRm5OUJ2hi5MvD0vGa8cTFXE-JsPwfFqYw130_assertion
dcterms:description
"[In the present study, we found MyD88-deficient mice fed a HFD had increased circulating levels of insulin, leptin and cholesterol, as well as liver dysfunction (increased induction of ALT levels, increased activation of JNK and cleavage of PARP), which were linked to the onset of severe diabetes.]. 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:20824098
;
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:NP886111.RAeQ8JRMF61sRm5OUJ2hi5MvD0vGa8cTFXE-JsPwfFqYw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:01+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" .
}