@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP931332.RA6gBLBdMXwSp2gu5MXpeAwi9ZBy-QMWnEGRq8uqG1CLg
> .
@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:NP931332.RA6gBLBdMXwSp2gu5MXpeAwi9ZBy-QMWnEGRq8uqG1CLg130_head
{
this:
np:hasAssertion
dgn-np:NP931332.RA6gBLBdMXwSp2gu5MXpeAwi9ZBy-QMWnEGRq8uqG1CLg130_assertion
;
np:hasProvenance
dgn-np:NP931332.RA6gBLBdMXwSp2gu5MXpeAwi9ZBy-QMWnEGRq8uqG1CLg130_provenance
;
np:hasPublicationInfo
dgn-np:NP931332.RA6gBLBdMXwSp2gu5MXpeAwi9ZBy-QMWnEGRq8uqG1CLg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP931332.RA6gBLBdMXwSp2gu5MXpeAwi9ZBy-QMWnEGRq8uqG1CLg130_assertion
a
np:Assertion
.
dgn-np:NP931332.RA6gBLBdMXwSp2gu5MXpeAwi9ZBy-QMWnEGRq8uqG1CLg130_provenance
a
np:Provenance
.
dgn-np:NP931332.RA6gBLBdMXwSp2gu5MXpeAwi9ZBy-QMWnEGRq8uqG1CLg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP931332.RA6gBLBdMXwSp2gu5MXpeAwi9ZBy-QMWnEGRq8uqG1CLg130_assertion
{
miriam-gene:121278
a
ncit:C16612
.
lld:C1839839
a
ncit:C7057
.
dgn-gda:DGN3b97502399d60f7c99b82e0b187cb939
sio:SIO_000628
miriam-gene:121278
,
lld:C1839839
;
a
sio:SIO_001121
.
}
dgn-np:NP931332.RA6gBLBdMXwSp2gu5MXpeAwi9ZBy-QMWnEGRq8uqG1CLg130_provenance
{
dgn-np:NP931332.RA6gBLBdMXwSp2gu5MXpeAwi9ZBy-QMWnEGRq8uqG1CLg130_assertion
dcterms:description
"[In order to assess the possible contribution of TPH2 genetic variability to the aetiology of bipolar affective disorder (BPAD), we systematically investigated common and rare genetic variation in the TPH2 gene through a sequential sequencing and SNP-based genotyping approach.]. 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:17905754
;
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:NP931332.RA6gBLBdMXwSp2gu5MXpeAwi9ZBy-QMWnEGRq8uqG1CLg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:31+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" .
}