@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP92183.RAOMWhpvU-aVMlD6vmiDbOYzr3H8wFZJE6LNcC_1nTmtM
> .
@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:NP92183.RAOMWhpvU-aVMlD6vmiDbOYzr3H8wFZJE6LNcC_1nTmtM130_head
{
this:
np:hasAssertion
dgn-np:NP92183.RAOMWhpvU-aVMlD6vmiDbOYzr3H8wFZJE6LNcC_1nTmtM130_assertion
;
np:hasProvenance
dgn-np:NP92183.RAOMWhpvU-aVMlD6vmiDbOYzr3H8wFZJE6LNcC_1nTmtM130_provenance
;
np:hasPublicationInfo
dgn-np:NP92183.RAOMWhpvU-aVMlD6vmiDbOYzr3H8wFZJE6LNcC_1nTmtM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP92183.RAOMWhpvU-aVMlD6vmiDbOYzr3H8wFZJE6LNcC_1nTmtM130_assertion
a
np:Assertion
.
dgn-np:NP92183.RAOMWhpvU-aVMlD6vmiDbOYzr3H8wFZJE6LNcC_1nTmtM130_provenance
a
np:Provenance
.
dgn-np:NP92183.RAOMWhpvU-aVMlD6vmiDbOYzr3H8wFZJE6LNcC_1nTmtM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP92183.RAOMWhpvU-aVMlD6vmiDbOYzr3H8wFZJE6LNcC_1nTmtM130_assertion
{
miriam-gene:6622
a
ncit:C16612
.
lld:C0752347
a
ncit:C7057
.
dgn-gda:DGN697437c20536d649556995bba876186b
sio:SIO_000628
miriam-gene:6622
,
lld:C0752347
;
a
sio:SIO_001122
.
}
dgn-np:NP92183.RAOMWhpvU-aVMlD6vmiDbOYzr3H8wFZJE6LNcC_1nTmtM130_provenance
{
dgn-np:NP92183.RAOMWhpvU-aVMlD6vmiDbOYzr3H8wFZJE6LNcC_1nTmtM130_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:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP92183.RAOMWhpvU-aVMlD6vmiDbOYzr3H8wFZJE6LNcC_1nTmtM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:45+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" .
}