@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP171269.RAC9YPxH3kBVHsWYqt5Iz6C6g53YdRCxRIFyeyWetcKmk
> .
@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:NP171269.RAC9YPxH3kBVHsWYqt5Iz6C6g53YdRCxRIFyeyWetcKmk130_head
{
this:
np:hasAssertion
dgn-np:NP171269.RAC9YPxH3kBVHsWYqt5Iz6C6g53YdRCxRIFyeyWetcKmk130_assertion
;
np:hasProvenance
dgn-np:NP171269.RAC9YPxH3kBVHsWYqt5Iz6C6g53YdRCxRIFyeyWetcKmk130_provenance
;
np:hasPublicationInfo
dgn-np:NP171269.RAC9YPxH3kBVHsWYqt5Iz6C6g53YdRCxRIFyeyWetcKmk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP171269.RAC9YPxH3kBVHsWYqt5Iz6C6g53YdRCxRIFyeyWetcKmk130_assertion
a
np:Assertion
.
dgn-np:NP171269.RAC9YPxH3kBVHsWYqt5Iz6C6g53YdRCxRIFyeyWetcKmk130_provenance
a
np:Provenance
.
dgn-np:NP171269.RAC9YPxH3kBVHsWYqt5Iz6C6g53YdRCxRIFyeyWetcKmk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP171269.RAC9YPxH3kBVHsWYqt5Iz6C6g53YdRCxRIFyeyWetcKmk130_assertion
{
miriam-gene:8021
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGN3c273ef0ee75fe9a8abb06dedb47c97e
sio:SIO_000628
miriam-gene:8021
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP171269.RAC9YPxH3kBVHsWYqt5Iz6C6g53YdRCxRIFyeyWetcKmk130_provenance
{
dgn-np:NP171269.RAC9YPxH3kBVHsWYqt5Iz6C6g53YdRCxRIFyeyWetcKmk130_assertion
dcterms:description
"[The evidence for this assertion is strongest in Parkinson's disease (PD), where genetic variability in alpha-synuclein expression affects risk of developing disease, although the oldest evidence for the notion that increased expression of normal sequence protein can lead to disease comes from the observation of Alzheimer's disease in trisomy 21 cases.]. 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:14976159
;
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:NP171269.RAC9YPxH3kBVHsWYqt5Iz6C6g53YdRCxRIFyeyWetcKmk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:32+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" .
}