@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP308096.RAmRk0le5oBv_uuKpUxG9D3o0cAaoAqnfn3t8nuV_I4Nc
> .
@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:NP308096.RAmRk0le5oBv_uuKpUxG9D3o0cAaoAqnfn3t8nuV_I4Nc130_head
{
this:
np:hasAssertion
dgn-np:NP308096.RAmRk0le5oBv_uuKpUxG9D3o0cAaoAqnfn3t8nuV_I4Nc130_assertion
;
np:hasProvenance
dgn-np:NP308096.RAmRk0le5oBv_uuKpUxG9D3o0cAaoAqnfn3t8nuV_I4Nc130_provenance
;
np:hasPublicationInfo
dgn-np:NP308096.RAmRk0le5oBv_uuKpUxG9D3o0cAaoAqnfn3t8nuV_I4Nc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP308096.RAmRk0le5oBv_uuKpUxG9D3o0cAaoAqnfn3t8nuV_I4Nc130_assertion
a
np:Assertion
.
dgn-np:NP308096.RAmRk0le5oBv_uuKpUxG9D3o0cAaoAqnfn3t8nuV_I4Nc130_provenance
a
np:Provenance
.
dgn-np:NP308096.RAmRk0le5oBv_uuKpUxG9D3o0cAaoAqnfn3t8nuV_I4Nc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP308096.RAmRk0le5oBv_uuKpUxG9D3o0cAaoAqnfn3t8nuV_I4Nc130_assertion
{
miriam-gene:3952
a
ncit:C16612
.
lld:C0011581
a
ncit:C7057
.
dgn-gda:DGN2b4e51d0f89b2cbe97d171497ca53a57
sio:SIO_000628
miriam-gene:3952
,
lld:C0011581
;
a
sio:SIO_001121
.
}
dgn-np:NP308096.RAmRk0le5oBv_uuKpUxG9D3o0cAaoAqnfn3t8nuV_I4Nc130_provenance
{
dgn-np:NP308096.RAmRk0le5oBv_uuKpUxG9D3o0cAaoAqnfn3t8nuV_I4Nc130_assertion
dcterms:description
"[Our results suggest an involvement of leptin in antidepressant action and cognitive function in depression with genetic polymorphisms in the leptin gene, decreased leptin gene expression and leptin deficiency in serum being risk factors for resistance to antidepressant therapy in depressed patients.]. 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:23026132
;
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:NP308096.RAmRk0le5oBv_uuKpUxG9D3o0cAaoAqnfn3t8nuV_I4Nc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:57+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" .
}