@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP588162.RAzszxW6VDfNzfj91OoSUljBqooEkHAl22UBGTFPBKlFo
> .
@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:NP588162.RAzszxW6VDfNzfj91OoSUljBqooEkHAl22UBGTFPBKlFo130_head
{
this:
np:hasAssertion
dgn-np:NP588162.RAzszxW6VDfNzfj91OoSUljBqooEkHAl22UBGTFPBKlFo130_assertion
;
np:hasProvenance
dgn-np:NP588162.RAzszxW6VDfNzfj91OoSUljBqooEkHAl22UBGTFPBKlFo130_provenance
;
np:hasPublicationInfo
dgn-np:NP588162.RAzszxW6VDfNzfj91OoSUljBqooEkHAl22UBGTFPBKlFo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP588162.RAzszxW6VDfNzfj91OoSUljBqooEkHAl22UBGTFPBKlFo130_assertion
a
np:Assertion
.
dgn-np:NP588162.RAzszxW6VDfNzfj91OoSUljBqooEkHAl22UBGTFPBKlFo130_provenance
a
np:Provenance
.
dgn-np:NP588162.RAzszxW6VDfNzfj91OoSUljBqooEkHAl22UBGTFPBKlFo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP588162.RAzszxW6VDfNzfj91OoSUljBqooEkHAl22UBGTFPBKlFo130_assertion
{
miriam-gene:6620
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGN3dcd5aded12f0837272da280fdb92258
sio:SIO_000628
miriam-gene:6620
,
lld:C0030567
;
a
sio:SIO_001121
.
}
dgn-np:NP588162.RAzszxW6VDfNzfj91OoSUljBqooEkHAl22UBGTFPBKlFo130_provenance
{
dgn-np:NP588162.RAzszxW6VDfNzfj91OoSUljBqooEkHAl22UBGTFPBKlFo130_assertion
dcterms:description
"[Our findings provide new insights into the pathogenesis of dementia in PD, indicating that differential BS and AS expression in the caudate nucleus may represent one of the molecular mechanisms involved in these complex diseases.]. 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:21683963
;
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:NP588162.RAzszxW6VDfNzfj91OoSUljBqooEkHAl22UBGTFPBKlFo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:54+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" .
}