@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP188486.RA9-jEa_d6k-UDZSU8MBIjDXf0XUKItAiHEydYdm1DXQw
> .
@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:NP188486.RA9-jEa_d6k-UDZSU8MBIjDXf0XUKItAiHEydYdm1DXQw130_head
{
this:
np:hasAssertion
dgn-np:NP188486.RA9-jEa_d6k-UDZSU8MBIjDXf0XUKItAiHEydYdm1DXQw130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP188486.RA9-jEa_d6k-UDZSU8MBIjDXf0XUKItAiHEydYdm1DXQw130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP188486.RA9-jEa_d6k-UDZSU8MBIjDXf0XUKItAiHEydYdm1DXQw130_assertion
a
np:Assertion
.
dgn-np:NP188486.RA9-jEa_d6k-UDZSU8MBIjDXf0XUKItAiHEydYdm1DXQw130_provenance
a
np:Provenance
.
dgn-np:NP188486.RA9-jEa_d6k-UDZSU8MBIjDXf0XUKItAiHEydYdm1DXQw130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:3356
a
ncit:C16612
.
lld:C0270328
a
ncit:C7057
.
dgn-gda:DGNe84c5005944178de4c4abe6fc8590568
sio:SIO_000628
miriam-gene:3356
,
lld:C0270328
;
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.
}
dgn-np:NP188486.RA9-jEa_d6k-UDZSU8MBIjDXf0XUKItAiHEydYdm1DXQw130_provenance
{
dgn-np:NP188486.RA9-jEa_d6k-UDZSU8MBIjDXf0XUKItAiHEydYdm1DXQw130_assertion
dcterms:description
"[This is the first study that shows the association between 5HTR2A gene polymorphisms and polysymptomatic NE. These results provide further evidence suggesting that genetic variations at 5HTR2A may influence NE treatment response.]. 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:21089166
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP188486.RA9-jEa_d6k-UDZSU8MBIjDXf0XUKItAiHEydYdm1DXQw130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:12+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
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;
pav:authoredBy
<
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> , <
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
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"v4.0.0" .
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