@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP179951.RANIu0dds68tmeUTPbCcr1MLeKYgdGacf3KkeXJCj0AUc
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP179951.RANIu0dds68tmeUTPbCcr1MLeKYgdGacf3KkeXJCj0AUc130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP179951.RANIu0dds68tmeUTPbCcr1MLeKYgdGacf3KkeXJCj0AUc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP179951.RANIu0dds68tmeUTPbCcr1MLeKYgdGacf3KkeXJCj0AUc130_assertion
a
np:Assertion
.
dgn-np:NP179951.RANIu0dds68tmeUTPbCcr1MLeKYgdGacf3KkeXJCj0AUc130_provenance
a
np:Provenance
.
dgn-np:NP179951.RANIu0dds68tmeUTPbCcr1MLeKYgdGacf3KkeXJCj0AUc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP179951.RANIu0dds68tmeUTPbCcr1MLeKYgdGacf3KkeXJCj0AUc130_assertion
{
miriam-gene:57030
a
ncit:C16612
.
lld:C0595905
a
ncit:C7057
.
dgn-gda:DGN2b65b447d9402d1b011c9783f7b31172
sio:SIO_000628
miriam-gene:57030
,
lld:C0595905
;
a
sio:SIO_001121
.
}
dgn-np:NP179951.RANIu0dds68tmeUTPbCcr1MLeKYgdGacf3KkeXJCj0AUc130_provenance
{
dgn-np:NP179951.RANIu0dds68tmeUTPbCcr1MLeKYgdGacf3KkeXJCj0AUc130_assertion
dcterms:description
"[In the hippocampus, the loss of VGLUT1 mRNA supports data indicating that glutamatergic presynaptic deficits are prominent, whereas the pattern of results in temporal and frontal cortex suggests broadly similar changes may affect inhibitory and excitatory neurons.]. 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:15653259
;
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:NP179951.RANIu0dds68tmeUTPbCcr1MLeKYgdGacf3KkeXJCj0AUc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:37+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" .
}