@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP772156.RAEdYwtG9fixb67Zj0HAWmJnBXqyrIpMoaxlbt3vuFJr4
> .
@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:NP772156.RAEdYwtG9fixb67Zj0HAWmJnBXqyrIpMoaxlbt3vuFJr4130_head
{
this:
np:hasAssertion
dgn-np:NP772156.RAEdYwtG9fixb67Zj0HAWmJnBXqyrIpMoaxlbt3vuFJr4130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP772156.RAEdYwtG9fixb67Zj0HAWmJnBXqyrIpMoaxlbt3vuFJr4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP772156.RAEdYwtG9fixb67Zj0HAWmJnBXqyrIpMoaxlbt3vuFJr4130_assertion
a
np:Assertion
.
dgn-np:NP772156.RAEdYwtG9fixb67Zj0HAWmJnBXqyrIpMoaxlbt3vuFJr4130_provenance
a
np:Provenance
.
dgn-np:NP772156.RAEdYwtG9fixb67Zj0HAWmJnBXqyrIpMoaxlbt3vuFJr4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP772156.RAEdYwtG9fixb67Zj0HAWmJnBXqyrIpMoaxlbt3vuFJr4130_assertion
{
miriam-gene:1565
a
ncit:C16612
.
lld:C0393571
a
ncit:C7057
.
dgn-gda:DGN7dfe5d09bdf6c2147f2e3a96afafa8c0
sio:SIO_000628
miriam-gene:1565
,
lld:C0393571
;
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.
}
dgn-np:NP772156.RAEdYwtG9fixb67Zj0HAWmJnBXqyrIpMoaxlbt3vuFJr4130_provenance
{
dgn-np:NP772156.RAEdYwtG9fixb67Zj0HAWmJnBXqyrIpMoaxlbt3vuFJr4130_assertion
dcterms:description
"[To investigate the relationship between CYP2D6 genotypes (reported to be associated with the susceptibilities to Parkinson's disease and multisystem atrophy) and the possible susceptibility to neuroleptic malignant syndrome (NMS) and subacute myelo-optico-neuropathy (SMON), we analyzed the CYP2D6 gene by polymerase chain reaction and restriction fragment length polymorphism in Japanese schizophrenia patients with a history of NMS.]. 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:9892857
;
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:NP772156.RAEdYwtG9fixb67Zj0HAWmJnBXqyrIpMoaxlbt3vuFJr4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:47+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
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pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
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> , <
http://orcid.org/0000-0002-9383-528X
> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
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}