@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP67142.RAjsv-FaY-dnTKBgBtKYs9CXu8sar8HZTq-sfJzhA5oQo
> .
@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:NP67142.RAjsv-FaY-dnTKBgBtKYs9CXu8sar8HZTq-sfJzhA5oQo130_head
{
this:
np:hasAssertion
dgn-np:NP67142.RAjsv-FaY-dnTKBgBtKYs9CXu8sar8HZTq-sfJzhA5oQo130_assertion
;
np:hasProvenance
dgn-np:NP67142.RAjsv-FaY-dnTKBgBtKYs9CXu8sar8HZTq-sfJzhA5oQo130_provenance
;
np:hasPublicationInfo
dgn-np:NP67142.RAjsv-FaY-dnTKBgBtKYs9CXu8sar8HZTq-sfJzhA5oQo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP67142.RAjsv-FaY-dnTKBgBtKYs9CXu8sar8HZTq-sfJzhA5oQo130_assertion
a
np:Assertion
.
dgn-np:NP67142.RAjsv-FaY-dnTKBgBtKYs9CXu8sar8HZTq-sfJzhA5oQo130_provenance
a
np:Provenance
.
dgn-np:NP67142.RAjsv-FaY-dnTKBgBtKYs9CXu8sar8HZTq-sfJzhA5oQo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP67142.RAjsv-FaY-dnTKBgBtKYs9CXu8sar8HZTq-sfJzhA5oQo130_assertion
{
miriam-gene:283871
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGN4483a1460fae77a1e681180f60a2302f
sio:SIO_000628
miriam-gene:283871
,
lld:C0036341
;
a
sio:SIO_001122
.
}
dgn-np:NP67142.RAjsv-FaY-dnTKBgBtKYs9CXu8sar8HZTq-sfJzhA5oQo130_provenance
{
dgn-np:NP67142.RAjsv-FaY-dnTKBgBtKYs9CXu8sar8HZTq-sfJzhA5oQo130_assertion
dcterms:description
"[The analysis using C1236T or G2677AT genotypes gave similar results, due to linkage of these polymorphisms.PGP polymorphisms may affect the penetration of olanzapine into the central nervous system as seen by a relationship between the 3435T allele, olanzapine plasma levels, and reduction in the positive symptoms of 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:17038883
;
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:NP67142.RAjsv-FaY-dnTKBgBtKYs9CXu8sar8HZTq-sfJzhA5oQo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:32+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" .
}