@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1253998.RAtutSpnXDbzhKj1R6EaRRkoTOa281WVMaOr_YbMzKLCw
> .
@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/v4.0.0/void/
> .
dgn-np:NP1253998.RAtutSpnXDbzhKj1R6EaRRkoTOa281WVMaOr_YbMzKLCw130_head
{
this:
np:hasAssertion
dgn-np:NP1253998.RAtutSpnXDbzhKj1R6EaRRkoTOa281WVMaOr_YbMzKLCw130_assertion
;
np:hasProvenance
dgn-np:NP1253998.RAtutSpnXDbzhKj1R6EaRRkoTOa281WVMaOr_YbMzKLCw130_provenance
;
np:hasPublicationInfo
dgn-np:NP1253998.RAtutSpnXDbzhKj1R6EaRRkoTOa281WVMaOr_YbMzKLCw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1253998.RAtutSpnXDbzhKj1R6EaRRkoTOa281WVMaOr_YbMzKLCw130_assertion
a
np:Assertion
.
dgn-np:NP1253998.RAtutSpnXDbzhKj1R6EaRRkoTOa281WVMaOr_YbMzKLCw130_provenance
a
np:Provenance
.
dgn-np:NP1253998.RAtutSpnXDbzhKj1R6EaRRkoTOa281WVMaOr_YbMzKLCw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1253998.RAtutSpnXDbzhKj1R6EaRRkoTOa281WVMaOr_YbMzKLCw130_assertion
{
miriam-gene:2629
a
ncit:C16612
.
lld:C0752347
a
ncit:C7057
.
dgn-gda:DGN2aa6e66cb716498a571011ff27b01a1e
sio:SIO_000628
miriam-gene:2629
,
lld:C0752347
;
a
sio:SIO_001121
.
}
dgn-np:NP1253998.RAtutSpnXDbzhKj1R6EaRRkoTOa281WVMaOr_YbMzKLCw130_provenance
{
dgn-np:NP1253998.RAtutSpnXDbzhKj1R6EaRRkoTOa281WVMaOr_YbMzKLCw130_assertion
dcterms:description
"[Despite the wealth of experimental, clinical and genetic evidence that supports the association between mutant genotypes and synucleinopathy risk, the precise mechanisms by which GBA1 mutations lead to PD and DLB remain unclear.]. 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:25573151
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1253998.RAtutSpnXDbzhKj1R6EaRRkoTOa281WVMaOr_YbMzKLCw130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:14+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}