@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP363466.RAdU4PY27Hlti4dk-1FTayCr57KlAhU3gMcSf7QeEpZ3E
> .
@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:NP363466.RAdU4PY27Hlti4dk-1FTayCr57KlAhU3gMcSf7QeEpZ3E130_head
{
this:
np:hasAssertion
dgn-np:NP363466.RAdU4PY27Hlti4dk-1FTayCr57KlAhU3gMcSf7QeEpZ3E130_assertion
;
np:hasProvenance
dgn-np:NP363466.RAdU4PY27Hlti4dk-1FTayCr57KlAhU3gMcSf7QeEpZ3E130_provenance
;
np:hasPublicationInfo
dgn-np:NP363466.RAdU4PY27Hlti4dk-1FTayCr57KlAhU3gMcSf7QeEpZ3E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP363466.RAdU4PY27Hlti4dk-1FTayCr57KlAhU3gMcSf7QeEpZ3E130_assertion
a
np:Assertion
.
dgn-np:NP363466.RAdU4PY27Hlti4dk-1FTayCr57KlAhU3gMcSf7QeEpZ3E130_provenance
a
np:Provenance
.
dgn-np:NP363466.RAdU4PY27Hlti4dk-1FTayCr57KlAhU3gMcSf7QeEpZ3E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP363466.RAdU4PY27Hlti4dk-1FTayCr57KlAhU3gMcSf7QeEpZ3E130_assertion
{
miriam-gene:3358
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGN1c775087075a5c8921fc9c0b6fce1559
sio:SIO_000628
miriam-gene:3358
,
lld:C0036341
;
a
sio:SIO_001121
.
}
dgn-np:NP363466.RAdU4PY27Hlti4dk-1FTayCr57KlAhU3gMcSf7QeEpZ3E130_provenance
{
dgn-np:NP363466.RAdU4PY27Hlti4dk-1FTayCr57KlAhU3gMcSf7QeEpZ3E130_assertion
dcterms:description
"[Screening of the 5-HT(2C)R gene did not reveal any mutations likely to disrupt the dsRNA loop, suggesting that the reduced RNA editing in schizophrenia may instead be caused by altered activity of the editing enzyme(s).]. 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:11443520
;
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:NP363466.RAdU4PY27Hlti4dk-1FTayCr57KlAhU3gMcSf7QeEpZ3E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:33+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" .
}