@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP609952.RA6yc8wYYWRvu9CLL9wyhJwLaG3U--i9TFcuW8kLfaioQ
> .
@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:NP609952.RA6yc8wYYWRvu9CLL9wyhJwLaG3U--i9TFcuW8kLfaioQ130_head
{
this:
np:hasAssertion
dgn-np:NP609952.RA6yc8wYYWRvu9CLL9wyhJwLaG3U--i9TFcuW8kLfaioQ130_assertion
;
np:hasProvenance
dgn-np:NP609952.RA6yc8wYYWRvu9CLL9wyhJwLaG3U--i9TFcuW8kLfaioQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP609952.RA6yc8wYYWRvu9CLL9wyhJwLaG3U--i9TFcuW8kLfaioQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP609952.RA6yc8wYYWRvu9CLL9wyhJwLaG3U--i9TFcuW8kLfaioQ130_assertion
a
np:Assertion
.
dgn-np:NP609952.RA6yc8wYYWRvu9CLL9wyhJwLaG3U--i9TFcuW8kLfaioQ130_provenance
a
np:Provenance
.
dgn-np:NP609952.RA6yc8wYYWRvu9CLL9wyhJwLaG3U--i9TFcuW8kLfaioQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP609952.RA6yc8wYYWRvu9CLL9wyhJwLaG3U--i9TFcuW8kLfaioQ130_assertion
{
miriam-gene:5079
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGNc703424b173de3e137b863e7b47fc0c4
sio:SIO_000628
miriam-gene:5079
,
lld:C0030567
;
a
sio:SIO_001122
.
}
dgn-np:NP609952.RA6yc8wYYWRvu9CLL9wyhJwLaG3U--i9TFcuW8kLfaioQ130_provenance
{
dgn-np:NP609952.RA6yc8wYYWRvu9CLL9wyhJwLaG3U--i9TFcuW8kLfaioQ130_assertion
dcterms:description
"[These findings suggest that variants in all 3 members of the synuclein gene family, particularly SNCA and SNCG, affect the risk of developing DLBD and warrant further investigation in larger, pathologically defined data sets as well as clinically diagnosed Parkinson disease/dementia with Lewy bodies case-control series.]. 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:20697047
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP609952.RA6yc8wYYWRvu9CLL9wyhJwLaG3U--i9TFcuW8kLfaioQ130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:43:44+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" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}