@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP579062.RAoLR4JtoU79JXGmpWV-q0xjCiVnoxV4uzhRDBu45Wyec
> .
@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:NP579062.RAoLR4JtoU79JXGmpWV-q0xjCiVnoxV4uzhRDBu45Wyec130_assertion
;
np:hasProvenance
dgn-np:NP579062.RAoLR4JtoU79JXGmpWV-q0xjCiVnoxV4uzhRDBu45Wyec130_provenance
;
np:hasPublicationInfo
dgn-np:NP579062.RAoLR4JtoU79JXGmpWV-q0xjCiVnoxV4uzhRDBu45Wyec130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP579062.RAoLR4JtoU79JXGmpWV-q0xjCiVnoxV4uzhRDBu45Wyec130_assertion
a
np:Assertion
.
dgn-np:NP579062.RAoLR4JtoU79JXGmpWV-q0xjCiVnoxV4uzhRDBu45Wyec130_provenance
a
np:Provenance
.
dgn-np:NP579062.RAoLR4JtoU79JXGmpWV-q0xjCiVnoxV4uzhRDBu45Wyec130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP579062.RAoLR4JtoU79JXGmpWV-q0xjCiVnoxV4uzhRDBu45Wyec130_assertion
{
miriam-gene:1565
a
ncit:C16612
.
lld:C0393571
a
ncit:C7057
.
dgn-gda:DGNae500c1ff95ebf727abf00299ceb9de0
sio:SIO_000628
miriam-gene:1565
,
lld:C0393571
;
a
sio:SIO_001121
.
}
dgn-np:NP579062.RAoLR4JtoU79JXGmpWV-q0xjCiVnoxV4uzhRDBu45Wyec130_provenance
{
dgn-np:NP579062.RAoLR4JtoU79JXGmpWV-q0xjCiVnoxV4uzhRDBu45Wyec130_assertion
dcterms:description
"[We have investigated CYP2D6 polymorphism in 91 patients with multiple system atrophy (MSA) in order to determine if this finding is specific to PD or if there is similar evidence of genetic susceptibility to neurotoxicity in MSA.]. 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:7651442
;
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:NP579062.RAoLR4JtoU79JXGmpWV-q0xjCiVnoxV4uzhRDBu45Wyec130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:49+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" .
}