@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP313370.RA3uCsuFAeVw8Dw7_-yczLBBAlWJAfnJIkYJX8ZgAKnxA
> .
@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:NP313370.RA3uCsuFAeVw8Dw7_-yczLBBAlWJAfnJIkYJX8ZgAKnxA130_head
{
this:
np:hasAssertion
dgn-np:NP313370.RA3uCsuFAeVw8Dw7_-yczLBBAlWJAfnJIkYJX8ZgAKnxA130_assertion
;
np:hasProvenance
dgn-np:NP313370.RA3uCsuFAeVw8Dw7_-yczLBBAlWJAfnJIkYJX8ZgAKnxA130_provenance
;
np:hasPublicationInfo
dgn-np:NP313370.RA3uCsuFAeVw8Dw7_-yczLBBAlWJAfnJIkYJX8ZgAKnxA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP313370.RA3uCsuFAeVw8Dw7_-yczLBBAlWJAfnJIkYJX8ZgAKnxA130_assertion
a
np:Assertion
.
dgn-np:NP313370.RA3uCsuFAeVw8Dw7_-yczLBBAlWJAfnJIkYJX8ZgAKnxA130_provenance
a
np:Provenance
.
dgn-np:NP313370.RA3uCsuFAeVw8Dw7_-yczLBBAlWJAfnJIkYJX8ZgAKnxA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP313370.RA3uCsuFAeVw8Dw7_-yczLBBAlWJAfnJIkYJX8ZgAKnxA130_assertion
{
miriam-gene:120892
a
ncit:C16612
.
lld:C0242422
a
ncit:C7057
.
dgn-gda:DGNab2f6c9a48dcbd43008f2ce46a678939
sio:SIO_000628
miriam-gene:120892
,
lld:C0242422
;
a
sio:SIO_001121
.
}
dgn-np:NP313370.RA3uCsuFAeVw8Dw7_-yczLBBAlWJAfnJIkYJX8ZgAKnxA130_provenance
{
dgn-np:NP313370.RA3uCsuFAeVw8Dw7_-yczLBBAlWJAfnJIkYJX8ZgAKnxA130_assertion
dcterms:description
"[The reasons for the selective predisposition of patients with mutations in LRRK2 to develop parkinsonism remains unclear, but Lrrk2 mutations may prime select neuronal populations to cellular insults that can lead to aberrant protein aggregation.]. 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:16437584
;
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:NP313370.RA3uCsuFAeVw8Dw7_-yczLBBAlWJAfnJIkYJX8ZgAKnxA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:59+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" .
}