@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP267092.RAZ982NzvhNWL1oLMXKjZB2g03grDEEPpf-ZDrwGiZ1BY
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP267092.RAZ982NzvhNWL1oLMXKjZB2g03grDEEPpf-ZDrwGiZ1BY130_assertion
;
np:hasProvenance
dgn-np:NP267092.RAZ982NzvhNWL1oLMXKjZB2g03grDEEPpf-ZDrwGiZ1BY130_provenance
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np:hasPublicationInfo
dgn-np:NP267092.RAZ982NzvhNWL1oLMXKjZB2g03grDEEPpf-ZDrwGiZ1BY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP267092.RAZ982NzvhNWL1oLMXKjZB2g03grDEEPpf-ZDrwGiZ1BY130_assertion
a
np:Assertion
.
dgn-np:NP267092.RAZ982NzvhNWL1oLMXKjZB2g03grDEEPpf-ZDrwGiZ1BY130_provenance
a
np:Provenance
.
dgn-np:NP267092.RAZ982NzvhNWL1oLMXKjZB2g03grDEEPpf-ZDrwGiZ1BY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP267092.RAZ982NzvhNWL1oLMXKjZB2g03grDEEPpf-ZDrwGiZ1BY130_assertion
{
miriam-gene:1565
a
ncit:C16612
.
lld:C0686347
a
ncit:C7057
.
dgn-gda:DGN274e0b16bd8fc171b0172c6e7a07989a
sio:SIO_000628
miriam-gene:1565
,
lld:C0686347
;
a
sio:SIO_001121
.
}
dgn-np:NP267092.RAZ982NzvhNWL1oLMXKjZB2g03grDEEPpf-ZDrwGiZ1BY130_provenance
{
dgn-np:NP267092.RAZ982NzvhNWL1oLMXKjZB2g03grDEEPpf-ZDrwGiZ1BY130_assertion
dcterms:description
"[We concluded that the CYP2D6*10 C188T polymorphism may be associated with the susceptibility to the occurrence of TD induced by typical antipsychotics, especially in male patients, and may also be correlated with AIMS scores in TD patients.]. 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:15118351
;
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 .
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dgn-np:NP267092.RAZ982NzvhNWL1oLMXKjZB2g03grDEEPpf-ZDrwGiZ1BY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:29+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
<
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> , <
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" .
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}