@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP43674.RAo-9b71p3pqlkyBjYZQvziKYn8C1tT2yEsgTekWpKeYc
> .
@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 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:NP43674.RAo-9b71p3pqlkyBjYZQvziKYn8C1tT2yEsgTekWpKeYc130_head
{
this:
np:hasAssertion
dgn-np:NP43674.RAo-9b71p3pqlkyBjYZQvziKYn8C1tT2yEsgTekWpKeYc130_assertion
;
np:hasProvenance
dgn-np:NP43674.RAo-9b71p3pqlkyBjYZQvziKYn8C1tT2yEsgTekWpKeYc130_provenance
;
np:hasPublicationInfo
dgn-np:NP43674.RAo-9b71p3pqlkyBjYZQvziKYn8C1tT2yEsgTekWpKeYc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP43674.RAo-9b71p3pqlkyBjYZQvziKYn8C1tT2yEsgTekWpKeYc130_assertion
a
np:Assertion
.
dgn-np:NP43674.RAo-9b71p3pqlkyBjYZQvziKYn8C1tT2yEsgTekWpKeYc130_provenance
a
np:Provenance
.
dgn-np:NP43674.RAo-9b71p3pqlkyBjYZQvziKYn8C1tT2yEsgTekWpKeYc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP43674.RAo-9b71p3pqlkyBjYZQvziKYn8C1tT2yEsgTekWpKeYc130_assertion
{
miriam-gene:2629
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGN9113925ca19ed0b1aae74439cf460978
sio:SIO_000628
miriam-gene:2629
,
lld:C0030567
;
a
sio:SIO_001122
.
}
dgn-np:NP43674.RAo-9b71p3pqlkyBjYZQvziKYn8C1tT2yEsgTekWpKeYc130_provenance
{
dgn-np:NP43674.RAo-9b71p3pqlkyBjYZQvziKYn8C1tT2yEsgTekWpKeYc130_assertion
dct:description
"[To characterize sequence variation within the glucocerebrosidase (GBA) gene in a select subset of our sample of patients with familial Parkinson disease (PD) and then to test in our full sample whether these sequence variants increased the risk for PD and were associated with an earlier onset of disease.]. 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:18987351
;
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:NP43674.RAo-9b71p3pqlkyBjYZQvziKYn8C1tT2yEsgTekWpKeYc130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:20+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}