@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP485230.RAUHdkcz3SK9zv13ukBnBcdop29cWKti7XYmNXStGTUek
> .
@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:NP485230.RAUHdkcz3SK9zv13ukBnBcdop29cWKti7XYmNXStGTUek130_head
{
this:
np:hasAssertion
dgn-np:NP485230.RAUHdkcz3SK9zv13ukBnBcdop29cWKti7XYmNXStGTUek130_assertion
;
np:hasProvenance
dgn-np:NP485230.RAUHdkcz3SK9zv13ukBnBcdop29cWKti7XYmNXStGTUek130_provenance
;
np:hasPublicationInfo
dgn-np:NP485230.RAUHdkcz3SK9zv13ukBnBcdop29cWKti7XYmNXStGTUek130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP485230.RAUHdkcz3SK9zv13ukBnBcdop29cWKti7XYmNXStGTUek130_assertion
a
np:Assertion
.
dgn-np:NP485230.RAUHdkcz3SK9zv13ukBnBcdop29cWKti7XYmNXStGTUek130_provenance
a
np:Provenance
.
dgn-np:NP485230.RAUHdkcz3SK9zv13ukBnBcdop29cWKti7XYmNXStGTUek130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP485230.RAUHdkcz3SK9zv13ukBnBcdop29cWKti7XYmNXStGTUek130_assertion
{
miriam-gene:27074
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGNff9019ae7ba1f50a8a19d75fbe822dca
sio:SIO_000628
miriam-gene:27074
,
lld:C0030567
;
a
sio:SIO_001121
.
}
dgn-np:NP485230.RAUHdkcz3SK9zv13ukBnBcdop29cWKti7XYmNXStGTUek130_provenance
{
dgn-np:NP485230.RAUHdkcz3SK9zv13ukBnBcdop29cWKti7XYmNXStGTUek130_assertion
dcterms:description
"[Subgroup analysis by ethnicity showed significantly stronger effects for the BST1 (rs11724635) in Asian vs Caucasian populations and similar effects for SNCA, LRRK2, LAMP3, HIP1R, and STK39 in Asian and Caucasian populations, while MAPT rs2942168 and SYT11 rs34372695 were monomorphic in the Asian population, highlighting the role of population-specific heterogeneity in PD.]. 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:22786590
;
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:NP485230.RAUHdkcz3SK9zv13ukBnBcdop29cWKti7XYmNXStGTUek130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:50+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" .
}