@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP687815.RAeXiMAYr-tvKOsPAEOPAj6Pug4HN8nZ6VJMY2KH-wOEk
> .
@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:NP687815.RAeXiMAYr-tvKOsPAEOPAj6Pug4HN8nZ6VJMY2KH-wOEk130_head
{
this:
np:hasAssertion
dgn-np:NP687815.RAeXiMAYr-tvKOsPAEOPAj6Pug4HN8nZ6VJMY2KH-wOEk130_assertion
;
np:hasProvenance
dgn-np:NP687815.RAeXiMAYr-tvKOsPAEOPAj6Pug4HN8nZ6VJMY2KH-wOEk130_provenance
;
np:hasPublicationInfo
dgn-np:NP687815.RAeXiMAYr-tvKOsPAEOPAj6Pug4HN8nZ6VJMY2KH-wOEk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP687815.RAeXiMAYr-tvKOsPAEOPAj6Pug4HN8nZ6VJMY2KH-wOEk130_assertion
a
np:Assertion
.
dgn-np:NP687815.RAeXiMAYr-tvKOsPAEOPAj6Pug4HN8nZ6VJMY2KH-wOEk130_provenance
a
np:Provenance
.
dgn-np:NP687815.RAeXiMAYr-tvKOsPAEOPAj6Pug4HN8nZ6VJMY2KH-wOEk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP687815.RAeXiMAYr-tvKOsPAEOPAj6Pug4HN8nZ6VJMY2KH-wOEk130_assertion
{
miriam-gene:120892
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGNcbb7d522e6726d8ef6218a38414f66f5
sio:SIO_000628
miriam-gene:120892
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP687815.RAeXiMAYr-tvKOsPAEOPAj6Pug4HN8nZ6VJMY2KH-wOEk130_provenance
{
dgn-np:NP687815.RAeXiMAYr-tvKOsPAEOPAj6Pug4HN8nZ6VJMY2KH-wOEk130_assertion
dcterms:description
"[While further evaluation is warranted, our findings indicate an increased risk of nonskin cancers in LRRK2 G2019S mutation carriers, which may be related to toxic gain of function of mutated LRRK2.]. 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:20818610
;
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:NP687815.RAeXiMAYr-tvKOsPAEOPAj6Pug4HN8nZ6VJMY2KH-wOEk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:58+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" .
}