@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP564633.RA6IlsvkoBmFTjgcYPF_a1FjhbDK3YWsMXh5lGa7ES8dE
> .
@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:NP564633.RA6IlsvkoBmFTjgcYPF_a1FjhbDK3YWsMXh5lGa7ES8dE130_head
{
this:
np:hasAssertion
dgn-np:NP564633.RA6IlsvkoBmFTjgcYPF_a1FjhbDK3YWsMXh5lGa7ES8dE130_assertion
;
np:hasProvenance
dgn-np:NP564633.RA6IlsvkoBmFTjgcYPF_a1FjhbDK3YWsMXh5lGa7ES8dE130_provenance
;
np:hasPublicationInfo
dgn-np:NP564633.RA6IlsvkoBmFTjgcYPF_a1FjhbDK3YWsMXh5lGa7ES8dE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP564633.RA6IlsvkoBmFTjgcYPF_a1FjhbDK3YWsMXh5lGa7ES8dE130_assertion
a
np:Assertion
.
dgn-np:NP564633.RA6IlsvkoBmFTjgcYPF_a1FjhbDK3YWsMXh5lGa7ES8dE130_provenance
a
np:Provenance
.
dgn-np:NP564633.RA6IlsvkoBmFTjgcYPF_a1FjhbDK3YWsMXh5lGa7ES8dE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP564633.RA6IlsvkoBmFTjgcYPF_a1FjhbDK3YWsMXh5lGa7ES8dE130_assertion
{
miriam-gene:120892
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGN2051eb6f16f4ad3ed03562e6fbbd8dd3
sio:SIO_000628
miriam-gene:120892
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP564633.RA6IlsvkoBmFTjgcYPF_a1FjhbDK3YWsMXh5lGa7ES8dE130_provenance
{
dgn-np:NP564633.RA6IlsvkoBmFTjgcYPF_a1FjhbDK3YWsMXh5lGa7ES8dE130_assertion
dcterms:description
"[In light of recent findings about the wide role of LRRK2 under normal and pathological conditions, it is tempting to speculate that LRRK2 mutations might play an upstream influence on the etiology of not just PD but also several alpha-synuclein and tau pathologies, including AD.]. 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:19072560
;
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:NP564633.RA6IlsvkoBmFTjgcYPF_a1FjhbDK3YWsMXh5lGa7ES8dE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:40+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" .
}