@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP66367.RAy4FfiYPE5AFlOLtAxJ421_i9yMEQTpsB5oIYQhtPUCM
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP66367.RAy4FfiYPE5AFlOLtAxJ421_i9yMEQTpsB5oIYQhtPUCM130_head
{
this:
np:hasAssertion
dgn-np:NP66367.RAy4FfiYPE5AFlOLtAxJ421_i9yMEQTpsB5oIYQhtPUCM130_assertion
;
np:hasProvenance
dgn-np:NP66367.RAy4FfiYPE5AFlOLtAxJ421_i9yMEQTpsB5oIYQhtPUCM130_provenance
;
np:hasPublicationInfo
dgn-np:NP66367.RAy4FfiYPE5AFlOLtAxJ421_i9yMEQTpsB5oIYQhtPUCM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP66367.RAy4FfiYPE5AFlOLtAxJ421_i9yMEQTpsB5oIYQhtPUCM130_assertion
a
np:Assertion
.
dgn-np:NP66367.RAy4FfiYPE5AFlOLtAxJ421_i9yMEQTpsB5oIYQhtPUCM130_provenance
a
np:Provenance
.
dgn-np:NP66367.RAy4FfiYPE5AFlOLtAxJ421_i9yMEQTpsB5oIYQhtPUCM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP66367.RAy4FfiYPE5AFlOLtAxJ421_i9yMEQTpsB5oIYQhtPUCM130_assertion
{
miriam-gene:5444
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGNdd4ee912287f313b19f5433ee8158f71
sio:SIO_000628
miriam-gene:5444
,
lld:C0030567
;
a
sio:SIO_001122
.
}
dgn-np:NP66367.RAy4FfiYPE5AFlOLtAxJ421_i9yMEQTpsB5oIYQhtPUCM130_provenance
{
dgn-np:NP66367.RAy4FfiYPE5AFlOLtAxJ421_i9yMEQTpsB5oIYQhtPUCM130_assertion
dcterms:description
"[The results of our study suggest that the genotypes A/A and M/M genes of CYP2D6 and PON1, and allele epsilon4 gene are an important risk for the development of PD, causing its early onset. The cumulative effects of the risk genes cause an early onset of P]. 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:17304721
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP66367.RAy4FfiYPE5AFlOLtAxJ421_i9yMEQTpsB5oIYQhtPUCM130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:16+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
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pav:version
"v3.0.0" .
}