@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP53349.RA-Kkmybb9a9aR_NC1aKi1Lj6RYQkRra_Ty0cPeW91Wf8
> .
@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:NP53349.RA-Kkmybb9a9aR_NC1aKi1Lj6RYQkRra_Ty0cPeW91Wf8130_head
{
this:
np:hasAssertion
dgn-np:NP53349.RA-Kkmybb9a9aR_NC1aKi1Lj6RYQkRra_Ty0cPeW91Wf8130_assertion
;
np:hasProvenance
dgn-np:NP53349.RA-Kkmybb9a9aR_NC1aKi1Lj6RYQkRra_Ty0cPeW91Wf8130_provenance
;
np:hasPublicationInfo
dgn-np:NP53349.RA-Kkmybb9a9aR_NC1aKi1Lj6RYQkRra_Ty0cPeW91Wf8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP53349.RA-Kkmybb9a9aR_NC1aKi1Lj6RYQkRra_Ty0cPeW91Wf8130_assertion
a
np:Assertion
.
dgn-np:NP53349.RA-Kkmybb9a9aR_NC1aKi1Lj6RYQkRra_Ty0cPeW91Wf8130_provenance
a
np:Provenance
.
dgn-np:NP53349.RA-Kkmybb9a9aR_NC1aKi1Lj6RYQkRra_Ty0cPeW91Wf8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP53349.RA-Kkmybb9a9aR_NC1aKi1Lj6RYQkRra_Ty0cPeW91Wf8130_assertion
{
miriam-gene:11315
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGNaae4de2b7f8203a3e495f13faa4da544
sio:SIO_000628
miriam-gene:11315
,
lld:C0030567
;
a
sio:SIO_001122
.
}
dgn-np:NP53349.RA-Kkmybb9a9aR_NC1aKi1Lj6RYQkRra_Ty0cPeW91Wf8130_provenance
{
dgn-np:NP53349.RA-Kkmybb9a9aR_NC1aKi1Lj6RYQkRra_Ty0cPeW91Wf8130_assertion
dcterms:description
"[The relative contribution of simple mutations and copy number variations (CNVs) in SNCA, PARK2, PINK1, PARK7, and LRRK2 to the genetic etiology of Parkinson disease (PD) is still unclear because most studies did not completely analyze each gene.]. 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:19405094
;
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:NP53349.RA-Kkmybb9a9aR_NC1aKi1Lj6RYQkRra_Ty0cPeW91Wf8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:24+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" .
}