@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP457918.RAN2Qjhz4ZvV-B7mku6GV3RMYxJaigDN_Sey0hRkAKEWs
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP457918.RAN2Qjhz4ZvV-B7mku6GV3RMYxJaigDN_Sey0hRkAKEWs130_head
{
this:
np:hasAssertion
dgn-np:NP457918.RAN2Qjhz4ZvV-B7mku6GV3RMYxJaigDN_Sey0hRkAKEWs130_assertion
;
np:hasProvenance
dgn-np:NP457918.RAN2Qjhz4ZvV-B7mku6GV3RMYxJaigDN_Sey0hRkAKEWs130_provenance
;
np:hasPublicationInfo
dgn-np:NP457918.RAN2Qjhz4ZvV-B7mku6GV3RMYxJaigDN_Sey0hRkAKEWs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP457918.RAN2Qjhz4ZvV-B7mku6GV3RMYxJaigDN_Sey0hRkAKEWs130_assertion
a
np:Assertion
.
dgn-np:NP457918.RAN2Qjhz4ZvV-B7mku6GV3RMYxJaigDN_Sey0hRkAKEWs130_provenance
a
np:Provenance
.
dgn-np:NP457918.RAN2Qjhz4ZvV-B7mku6GV3RMYxJaigDN_Sey0hRkAKEWs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP457918.RAN2Qjhz4ZvV-B7mku6GV3RMYxJaigDN_Sey0hRkAKEWs130_assertion
{
miriam-gene:4887
a
ncit:C16612
.
lld:C0036572
a
ncit:C7057
.
dgn-gda:DGN5a301a6d90336f7d2e5e6056bec55b77
sio:SIO_000628
miriam-gene:4887
,
lld:C0036572
;
a
sio:SIO_001121
.
}
dgn-np:NP457918.RAN2Qjhz4ZvV-B7mku6GV3RMYxJaigDN_Sey0hRkAKEWs130_provenance
{
dgn-np:NP457918.RAN2Qjhz4ZvV-B7mku6GV3RMYxJaigDN_Sey0hRkAKEWs130_assertion
dcterms:description
"[This concept is strongly supported by evidence that genetically modified rats overexpressing the NPY gene are less susceptible to seizures while deletion of NPY or Y2 receptor genes results in increased susceptibility to seizures.]. 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:15337376
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP457918.RAN2Qjhz4ZvV-B7mku6GV3RMYxJaigDN_Sey0hRkAKEWs130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:12+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}