@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP48637.RAhSvTWz9cUtETNOh5vtiHIvtyi2migtQSlX0PX438kEo
> .
@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 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:NP48637.RAhSvTWz9cUtETNOh5vtiHIvtyi2migtQSlX0PX438kEo130_head
{
this:
np:hasAssertion
dgn-np:NP48637.RAhSvTWz9cUtETNOh5vtiHIvtyi2migtQSlX0PX438kEo130_assertion
;
np:hasProvenance
dgn-np:NP48637.RAhSvTWz9cUtETNOh5vtiHIvtyi2migtQSlX0PX438kEo130_provenance
;
np:hasPublicationInfo
dgn-np:NP48637.RAhSvTWz9cUtETNOh5vtiHIvtyi2migtQSlX0PX438kEo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP48637.RAhSvTWz9cUtETNOh5vtiHIvtyi2migtQSlX0PX438kEo130_assertion
a
np:Assertion
.
dgn-np:NP48637.RAhSvTWz9cUtETNOh5vtiHIvtyi2migtQSlX0PX438kEo130_provenance
a
np:Provenance
.
dgn-np:NP48637.RAhSvTWz9cUtETNOh5vtiHIvtyi2migtQSlX0PX438kEo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP48637.RAhSvTWz9cUtETNOh5vtiHIvtyi2migtQSlX0PX438kEo130_assertion
{
miriam-gene:218
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGN05348741fa251de2d87d95d95d2b5b13
sio:SIO_000628
miriam-gene:218
,
lld:C0036341
;
a
sio:SIO_001122
.
}
dgn-np:NP48637.RAhSvTWz9cUtETNOh5vtiHIvtyi2migtQSlX0PX438kEo130_provenance
{
dgn-np:NP48637.RAhSvTWz9cUtETNOh5vtiHIvtyi2migtQSlX0PX438kEo130_assertion
dct:description
"[The present findings suggest that the COMT and ALDH3 combination may be the most common type involved in predisposing to schizophrenia. Since the combination blocks the whole pathways for the breakdown of DA and noradrenaline, it is very likely to play a central role in developing paranoid schizophrenia.]. 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:14745454
;
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:NP48637.RAhSvTWz9cUtETNOh5vtiHIvtyi2migtQSlX0PX438kEo130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:22+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}