@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP313482.RAI-5YS893kDeqxZRGsq1fShOYctC-kqTcqgEI17T4s00
> .
@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:NP313482.RAI-5YS893kDeqxZRGsq1fShOYctC-kqTcqgEI17T4s00130_head
{
this:
np:hasAssertion
dgn-np:NP313482.RAI-5YS893kDeqxZRGsq1fShOYctC-kqTcqgEI17T4s00130_assertion
;
np:hasProvenance
dgn-np:NP313482.RAI-5YS893kDeqxZRGsq1fShOYctC-kqTcqgEI17T4s00130_provenance
;
np:hasPublicationInfo
dgn-np:NP313482.RAI-5YS893kDeqxZRGsq1fShOYctC-kqTcqgEI17T4s00130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP313482.RAI-5YS893kDeqxZRGsq1fShOYctC-kqTcqgEI17T4s00130_assertion
a
np:Assertion
.
dgn-np:NP313482.RAI-5YS893kDeqxZRGsq1fShOYctC-kqTcqgEI17T4s00130_provenance
a
np:Provenance
.
dgn-np:NP313482.RAI-5YS893kDeqxZRGsq1fShOYctC-kqTcqgEI17T4s00130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP313482.RAI-5YS893kDeqxZRGsq1fShOYctC-kqTcqgEI17T4s00130_assertion
{
miriam-gene:1312
a
ncit:C16612
.
lld:C0003469
a
ncit:C7057
.
dgn-gda:DGNcc0318452291255056a8cf735d367cdd
sio:SIO_000628
miriam-gene:1312
,
lld:C0003469
;
a
sio:SIO_001121
.
}
dgn-np:NP313482.RAI-5YS893kDeqxZRGsq1fShOYctC-kqTcqgEI17T4s00130_provenance
{
dgn-np:NP313482.RAI-5YS893kDeqxZRGsq1fShOYctC-kqTcqgEI17T4s00130_assertion
dcterms:description
"[The existing studies consistently reveal strong genetic effects on the responsiveness of the fear circuit, particularly of genetic variants previously discussed as potential susceptibility variants for anxiety, e.g., the COMT 158val allele or the 5-HTTLPR short allele.]. 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:19944771
;
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:NP313482.RAI-5YS893kDeqxZRGsq1fShOYctC-kqTcqgEI17T4s00130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:59+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" .
}