@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP960252.RA067gqAlHFfi_lRf2vsLwvKju3VoIEYng_wCdTSaetXM
> .
@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:NP960252.RA067gqAlHFfi_lRf2vsLwvKju3VoIEYng_wCdTSaetXM130_head
{
this:
np:hasAssertion
dgn-np:NP960252.RA067gqAlHFfi_lRf2vsLwvKju3VoIEYng_wCdTSaetXM130_assertion
;
np:hasProvenance
dgn-np:NP960252.RA067gqAlHFfi_lRf2vsLwvKju3VoIEYng_wCdTSaetXM130_provenance
;
np:hasPublicationInfo
dgn-np:NP960252.RA067gqAlHFfi_lRf2vsLwvKju3VoIEYng_wCdTSaetXM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP960252.RA067gqAlHFfi_lRf2vsLwvKju3VoIEYng_wCdTSaetXM130_assertion
a
np:Assertion
.
dgn-np:NP960252.RA067gqAlHFfi_lRf2vsLwvKju3VoIEYng_wCdTSaetXM130_provenance
a
np:Provenance
.
dgn-np:NP960252.RA067gqAlHFfi_lRf2vsLwvKju3VoIEYng_wCdTSaetXM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP960252.RA067gqAlHFfi_lRf2vsLwvKju3VoIEYng_wCdTSaetXM130_assertion
{
miriam-gene:2629
a
ncit:C16612
.
lld:C0752347
a
ncit:C7057
.
dgn-gda:DGN0fd0d31d4542a8b9c5ee1740525bad02
sio:SIO_000628
miriam-gene:2629
,
lld:C0752347
;
a
sio:SIO_001121
.
}
dgn-np:NP960252.RA067gqAlHFfi_lRf2vsLwvKju3VoIEYng_wCdTSaetXM130_provenance
{
dgn-np:NP960252.RA067gqAlHFfi_lRf2vsLwvKju3VoIEYng_wCdTSaetXM130_assertion
dcterms:description
"[Despite the wealth of clinical and genetic evidence supporting 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:22327140
;
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:NP960252.RA067gqAlHFfi_lRf2vsLwvKju3VoIEYng_wCdTSaetXM130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:00+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" .
}