@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP55179.RAzWQyKefjNY_iC-kG3xFA2mB21kAJqID9V8P41g09258
> .
@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:NP55179.RAzWQyKefjNY_iC-kG3xFA2mB21kAJqID9V8P41g09258130_head
{
this:
np:hasAssertion
dgn-np:NP55179.RAzWQyKefjNY_iC-kG3xFA2mB21kAJqID9V8P41g09258130_assertion
;
np:hasProvenance
dgn-np:NP55179.RAzWQyKefjNY_iC-kG3xFA2mB21kAJqID9V8P41g09258130_provenance
;
np:hasPublicationInfo
dgn-np:NP55179.RAzWQyKefjNY_iC-kG3xFA2mB21kAJqID9V8P41g09258130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP55179.RAzWQyKefjNY_iC-kG3xFA2mB21kAJqID9V8P41g09258130_assertion
a
np:Assertion
.
dgn-np:NP55179.RAzWQyKefjNY_iC-kG3xFA2mB21kAJqID9V8P41g09258130_provenance
a
np:Provenance
.
dgn-np:NP55179.RAzWQyKefjNY_iC-kG3xFA2mB21kAJqID9V8P41g09258130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP55179.RAzWQyKefjNY_iC-kG3xFA2mB21kAJqID9V8P41g09258130_assertion
{
miriam-gene:120892
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGNd9419d44cef35fee4785a3a082b35421
sio:SIO_000628
miriam-gene:120892
,
lld:C0002395
;
a
sio:SIO_001122
.
}
dgn-np:NP55179.RAzWQyKefjNY_iC-kG3xFA2mB21kAJqID9V8P41g09258130_provenance
{
dgn-np:NP55179.RAzWQyKefjNY_iC-kG3xFA2mB21kAJqID9V8P41g09258130_assertion
dcterms:description
"[Nevertheless, these observations together with new information about the Lrrk2 critical multifunctionality do not rule out the possible influence of other variants within LRRK2 in AD, so that other screenings focusing in the whole extension of the LRRK2 using larger sized confirmed AD sample are urgently needed.]. 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:19822953
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP55179.RAzWQyKefjNY_iC-kG3xFA2mB21kAJqID9V8P41g09258130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:25+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" .
}