@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP30094.RAo6x5qwdo55U9AqaFShAbaMGpE0bftTclWYsiYurxAmQ
> .
@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:NP30094.RAo6x5qwdo55U9AqaFShAbaMGpE0bftTclWYsiYurxAmQ130_head
{
this:
np:hasAssertion
dgn-np:NP30094.RAo6x5qwdo55U9AqaFShAbaMGpE0bftTclWYsiYurxAmQ130_assertion
;
np:hasProvenance
dgn-np:NP30094.RAo6x5qwdo55U9AqaFShAbaMGpE0bftTclWYsiYurxAmQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP30094.RAo6x5qwdo55U9AqaFShAbaMGpE0bftTclWYsiYurxAmQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP30094.RAo6x5qwdo55U9AqaFShAbaMGpE0bftTclWYsiYurxAmQ130_assertion
a
np:Assertion
.
dgn-np:NP30094.RAo6x5qwdo55U9AqaFShAbaMGpE0bftTclWYsiYurxAmQ130_provenance
a
np:Provenance
.
dgn-np:NP30094.RAo6x5qwdo55U9AqaFShAbaMGpE0bftTclWYsiYurxAmQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP30094.RAo6x5qwdo55U9AqaFShAbaMGpE0bftTclWYsiYurxAmQ130_assertion
{
miriam-gene:6532
a
ncit:C16612
.
lld:C0005586
a
ncit:C7057
.
dgn-gda:DGNb57661cefc9a0b0ad2152a1bd78b94f2
sio:SIO_000628
miriam-gene:6532
,
lld:C0005586
;
a
sio:SIO_001121
.
}
dgn-np:NP30094.RAo6x5qwdo55U9AqaFShAbaMGpE0bftTclWYsiYurxAmQ130_provenance
{
dgn-np:NP30094.RAo6x5qwdo55U9AqaFShAbaMGpE0bftTclWYsiYurxAmQ130_assertion
dcterms:description
"[Relative to the comparison subjects, subjects with bipolar disorder without panic disorder, but not those with comorbid bipolar disorder and panic disorder, showed significantly higher frequencies of the COMT Met158 and the short 5-HTTLPR alleles and genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_curated
;
sio:SIO_000772
miriam-pubmed:11772685
;
prov:wasDerivedFrom
dgn-void:ctd_human-20130708
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:ctd_human-20130708
pav:importedOn
"2013-07-24"^^
xsd:date
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
}
dgn-np:NP30094.RAo6x5qwdo55U9AqaFShAbaMGpE0bftTclWYsiYurxAmQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:13+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" .
}