@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP903695.RAyACWdLUa3g0fcOffSCc2oEpA41Rl3-yIjR7pQVRmMFQ
> .
@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:NP903695.RAyACWdLUa3g0fcOffSCc2oEpA41Rl3-yIjR7pQVRmMFQ130_head
{
this:
np:hasAssertion
dgn-np:NP903695.RAyACWdLUa3g0fcOffSCc2oEpA41Rl3-yIjR7pQVRmMFQ130_assertion
;
np:hasProvenance
dgn-np:NP903695.RAyACWdLUa3g0fcOffSCc2oEpA41Rl3-yIjR7pQVRmMFQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP903695.RAyACWdLUa3g0fcOffSCc2oEpA41Rl3-yIjR7pQVRmMFQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP903695.RAyACWdLUa3g0fcOffSCc2oEpA41Rl3-yIjR7pQVRmMFQ130_assertion
a
np:Assertion
.
dgn-np:NP903695.RAyACWdLUa3g0fcOffSCc2oEpA41Rl3-yIjR7pQVRmMFQ130_provenance
a
np:Provenance
.
dgn-np:NP903695.RAyACWdLUa3g0fcOffSCc2oEpA41Rl3-yIjR7pQVRmMFQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP903695.RAyACWdLUa3g0fcOffSCc2oEpA41Rl3-yIjR7pQVRmMFQ130_assertion
{
miriam-gene:4852
a
ncit:C16612
.
lld:C0524620
a
ncit:C7057
.
dgn-gda:DGN40cda4ac7db1f88ffa3c70bb81484336
sio:SIO_000628
miriam-gene:4852
,
lld:C0524620
;
a
sio:SIO_001121
.
}
dgn-np:NP903695.RAyACWdLUa3g0fcOffSCc2oEpA41Rl3-yIjR7pQVRmMFQ130_provenance
{
dgn-np:NP903695.RAyACWdLUa3g0fcOffSCc2oEpA41Rl3-yIjR7pQVRmMFQ130_assertion
dcterms:description
"[High or low abundance of NPY and cognate receptors dysregulates the homeostatic milieu engendering hyperphagia, decreased energy expenditure, obesity and attendant metabolic syndrome cluster of dyslipidemia, glucose intolerance, insulin resistance and hyperinsulinemia, risk factors for type II diabetes and cardiovascular diseases.]. 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:16383005
;
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:NP903695.RAyACWdLUa3g0fcOffSCc2oEpA41Rl3-yIjR7pQVRmMFQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:15+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" .
}