@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP58804.RAaj5UQXcRCrvQIbEZMxQDbv-B0cC3SDEPOf0I_TwEOzQ
> .
@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:NP58804.RAaj5UQXcRCrvQIbEZMxQDbv-B0cC3SDEPOf0I_TwEOzQ130_head
{
this:
np:hasAssertion
dgn-np:NP58804.RAaj5UQXcRCrvQIbEZMxQDbv-B0cC3SDEPOf0I_TwEOzQ130_assertion
;
np:hasProvenance
dgn-np:NP58804.RAaj5UQXcRCrvQIbEZMxQDbv-B0cC3SDEPOf0I_TwEOzQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP58804.RAaj5UQXcRCrvQIbEZMxQDbv-B0cC3SDEPOf0I_TwEOzQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP58804.RAaj5UQXcRCrvQIbEZMxQDbv-B0cC3SDEPOf0I_TwEOzQ130_assertion
a
np:Assertion
.
dgn-np:NP58804.RAaj5UQXcRCrvQIbEZMxQDbv-B0cC3SDEPOf0I_TwEOzQ130_provenance
a
np:Provenance
.
dgn-np:NP58804.RAaj5UQXcRCrvQIbEZMxQDbv-B0cC3SDEPOf0I_TwEOzQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP58804.RAaj5UQXcRCrvQIbEZMxQDbv-B0cC3SDEPOf0I_TwEOzQ130_assertion
{
miriam-gene:7166
a
ncit:C16612
.
lld:C0152115
a
ncit:C7057
.
dgn-gda:DGNbd57012b9864230d847c88d9cae1dd79
sio:SIO_000628
miriam-gene:7166
,
lld:C0152115
;
a
sio:SIO_001122
.
}
dgn-np:NP58804.RAaj5UQXcRCrvQIbEZMxQDbv-B0cC3SDEPOf0I_TwEOzQ130_provenance
{
dgn-np:NP58804.RAaj5UQXcRCrvQIbEZMxQDbv-B0cC3SDEPOf0I_TwEOzQ130_assertion
dcterms:description
"[No significant associations were found. Within the limitations imposed by the size of the clinical sample, these findings suggest that the above polymorphic loci do not contribute significantly to risk for TD. Further examination of loci that yielded positive results at a trend level and investigation of other candidate genetic loci coding for antipsychotic drug targets is warranted.]. 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:14583797
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP58804.RAaj5UQXcRCrvQIbEZMxQDbv-B0cC3SDEPOf0I_TwEOzQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:27+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" .
}