@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP484690.RASVKV6WoaexDv1bTu7GM55qyxn-jjO2x9EhO2KZQz9Uw
> .
@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:NP484690.RASVKV6WoaexDv1bTu7GM55qyxn-jjO2x9EhO2KZQz9Uw130_head
{
this:
np:hasAssertion
dgn-np:NP484690.RASVKV6WoaexDv1bTu7GM55qyxn-jjO2x9EhO2KZQz9Uw130_assertion
;
np:hasProvenance
dgn-np:NP484690.RASVKV6WoaexDv1bTu7GM55qyxn-jjO2x9EhO2KZQz9Uw130_provenance
;
np:hasPublicationInfo
dgn-np:NP484690.RASVKV6WoaexDv1bTu7GM55qyxn-jjO2x9EhO2KZQz9Uw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP484690.RASVKV6WoaexDv1bTu7GM55qyxn-jjO2x9EhO2KZQz9Uw130_assertion
a
np:Assertion
.
dgn-np:NP484690.RASVKV6WoaexDv1bTu7GM55qyxn-jjO2x9EhO2KZQz9Uw130_provenance
a
np:Provenance
.
dgn-np:NP484690.RASVKV6WoaexDv1bTu7GM55qyxn-jjO2x9EhO2KZQz9Uw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP484690.RASVKV6WoaexDv1bTu7GM55qyxn-jjO2x9EhO2KZQz9Uw130_assertion
{
miriam-gene:5563
a
ncit:C16612
.
lld:C0028754
a
ncit:C7057
.
dgn-gda:DGN8ddf325ab7ad75e2ac2c811e20bf439d
sio:SIO_000628
miriam-gene:5563
,
lld:C0028754
;
a
sio:SIO_001121
.
}
dgn-np:NP484690.RASVKV6WoaexDv1bTu7GM55qyxn-jjO2x9EhO2KZQz9Uw130_provenance
{
dgn-np:NP484690.RASVKV6WoaexDv1bTu7GM55qyxn-jjO2x9EhO2KZQz9Uw130_assertion
dcterms:description
"[These data suggest that this impairment of leptin signaling in skeletal muscle may contribute to the aberrant regulation of fatty acid metabolism observed in obesity and that pharmacological activation of AMPK may be an effective therapy to bypass SOCS3-mediated skeletal muscle leptin resistance for the treatment of obesity-related disorders.]. 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:16822822
;
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:NP484690.RASVKV6WoaexDv1bTu7GM55qyxn-jjO2x9EhO2KZQz9Uw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:50+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" .
}