@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP651961.RARTzJUSqMAB3pQVnbhLkjdSxwcFl7Pus0BOwo32tTllo
> .
@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:NP651961.RARTzJUSqMAB3pQVnbhLkjdSxwcFl7Pus0BOwo32tTllo130_head
{
this:
np:hasAssertion
dgn-np:NP651961.RARTzJUSqMAB3pQVnbhLkjdSxwcFl7Pus0BOwo32tTllo130_assertion
;
np:hasProvenance
dgn-np:NP651961.RARTzJUSqMAB3pQVnbhLkjdSxwcFl7Pus0BOwo32tTllo130_provenance
;
np:hasPublicationInfo
dgn-np:NP651961.RARTzJUSqMAB3pQVnbhLkjdSxwcFl7Pus0BOwo32tTllo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP651961.RARTzJUSqMAB3pQVnbhLkjdSxwcFl7Pus0BOwo32tTllo130_assertion
a
np:Assertion
.
dgn-np:NP651961.RARTzJUSqMAB3pQVnbhLkjdSxwcFl7Pus0BOwo32tTllo130_provenance
a
np:Provenance
.
dgn-np:NP651961.RARTzJUSqMAB3pQVnbhLkjdSxwcFl7Pus0BOwo32tTllo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP651961.RARTzJUSqMAB3pQVnbhLkjdSxwcFl7Pus0BOwo32tTllo130_assertion
{
miriam-gene:1312
a
ncit:C16612
.
lld:C0338831
a
ncit:C7057
.
dgn-gda:DGNbb8d2d41799f19eb3c8961157b6d12c8
sio:SIO_000628
miriam-gene:1312
,
lld:C0338831
;
a
sio:SIO_001121
.
}
dgn-np:NP651961.RARTzJUSqMAB3pQVnbhLkjdSxwcFl7Pus0BOwo32tTllo130_provenance
{
dgn-np:NP651961.RARTzJUSqMAB3pQVnbhLkjdSxwcFl7Pus0BOwo32tTllo130_assertion
dcterms:description
"[64 BD type I patients (39 in manic and 25 in depressive episodes) and 75 healthy controls were genotyped for COMT rs4680 and assessed for FER using the Ekman 60 Faces (EK60) and Emotion Hexagon (Hx) tests.]. 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:22222175
;
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:NP651961.RARTzJUSqMAB3pQVnbhLkjdSxwcFl7Pus0BOwo32tTllo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:32+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" .
}