@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP230279.RA6GaFAif-rPht3SlrgKew2xxQ4hlyhNY69C37fsMEf9Q
> .
@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:NP230279.RA6GaFAif-rPht3SlrgKew2xxQ4hlyhNY69C37fsMEf9Q130_head
{
this:
np:hasAssertion
dgn-np:NP230279.RA6GaFAif-rPht3SlrgKew2xxQ4hlyhNY69C37fsMEf9Q130_assertion
;
np:hasProvenance
dgn-np:NP230279.RA6GaFAif-rPht3SlrgKew2xxQ4hlyhNY69C37fsMEf9Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP230279.RA6GaFAif-rPht3SlrgKew2xxQ4hlyhNY69C37fsMEf9Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP230279.RA6GaFAif-rPht3SlrgKew2xxQ4hlyhNY69C37fsMEf9Q130_assertion
a
np:Assertion
.
dgn-np:NP230279.RA6GaFAif-rPht3SlrgKew2xxQ4hlyhNY69C37fsMEf9Q130_provenance
a
np:Provenance
.
dgn-np:NP230279.RA6GaFAif-rPht3SlrgKew2xxQ4hlyhNY69C37fsMEf9Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP230279.RA6GaFAif-rPht3SlrgKew2xxQ4hlyhNY69C37fsMEf9Q130_assertion
{
miriam-gene:120892
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGNaaf40bc09127319eb0611c30648f5e65
sio:SIO_000628
miriam-gene:120892
,
lld:C0030567
;
a
sio:SIO_001122
.
}
dgn-np:NP230279.RA6GaFAif-rPht3SlrgKew2xxQ4hlyhNY69C37fsMEf9Q130_provenance
{
dgn-np:NP230279.RA6GaFAif-rPht3SlrgKew2xxQ4hlyhNY69C37fsMEf9Q130_assertion
dcterms:description
"[Our data suggest that the LRRK2 G2019S mutation plays an important role in the causality of familial and sporadic Parkinson disease (PD) in Israel and that gender affects its frequency among patients.]. 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:17938369
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP230279.RA6GaFAif-rPht3SlrgKew2xxQ4hlyhNY69C37fsMEf9Q130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:30+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" .
}