@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP209430.RAZto3MUMPU0sAiHK51Ji2iGdY5qEr9gvhCOM5NdTW6eQ
> .
@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:NP209430.RAZto3MUMPU0sAiHK51Ji2iGdY5qEr9gvhCOM5NdTW6eQ130_head
{
this:
np:hasAssertion
dgn-np:NP209430.RAZto3MUMPU0sAiHK51Ji2iGdY5qEr9gvhCOM5NdTW6eQ130_assertion
;
np:hasProvenance
dgn-np:NP209430.RAZto3MUMPU0sAiHK51Ji2iGdY5qEr9gvhCOM5NdTW6eQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP209430.RAZto3MUMPU0sAiHK51Ji2iGdY5qEr9gvhCOM5NdTW6eQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP209430.RAZto3MUMPU0sAiHK51Ji2iGdY5qEr9gvhCOM5NdTW6eQ130_assertion
a
np:Assertion
.
dgn-np:NP209430.RAZto3MUMPU0sAiHK51Ji2iGdY5qEr9gvhCOM5NdTW6eQ130_provenance
a
np:Provenance
.
dgn-np:NP209430.RAZto3MUMPU0sAiHK51Ji2iGdY5qEr9gvhCOM5NdTW6eQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP209430.RAZto3MUMPU0sAiHK51Ji2iGdY5qEr9gvhCOM5NdTW6eQ130_assertion
{
miriam-gene:4852
a
ncit:C16612
.
lld:C0007222
a
ncit:C7057
.
dgn-gda:DGNcb8a12771eb2492ca35bd55f9cdc175c
sio:SIO_000628
miriam-gene:4852
,
lld:C0007222
;
a
sio:SIO_001121
.
}
dgn-np:NP209430.RAZto3MUMPU0sAiHK51Ji2iGdY5qEr9gvhCOM5NdTW6eQ130_provenance
{
dgn-np:NP209430.RAZto3MUMPU0sAiHK51Ji2iGdY5qEr9gvhCOM5NdTW6eQ130_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:NP209430.RAZto3MUMPU0sAiHK51Ji2iGdY5qEr9gvhCOM5NdTW6eQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:55+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" .
}