@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP631470.RA5GKlp6nZmrz9gsaLaMgzESnxOoQyZ4LX9FeN03d6b3c
> .
@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:NP631470.RA5GKlp6nZmrz9gsaLaMgzESnxOoQyZ4LX9FeN03d6b3c130_head
{
this:
np:hasAssertion
dgn-np:NP631470.RA5GKlp6nZmrz9gsaLaMgzESnxOoQyZ4LX9FeN03d6b3c130_assertion
;
np:hasProvenance
dgn-np:NP631470.RA5GKlp6nZmrz9gsaLaMgzESnxOoQyZ4LX9FeN03d6b3c130_provenance
;
np:hasPublicationInfo
dgn-np:NP631470.RA5GKlp6nZmrz9gsaLaMgzESnxOoQyZ4LX9FeN03d6b3c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP631470.RA5GKlp6nZmrz9gsaLaMgzESnxOoQyZ4LX9FeN03d6b3c130_assertion
a
np:Assertion
.
dgn-np:NP631470.RA5GKlp6nZmrz9gsaLaMgzESnxOoQyZ4LX9FeN03d6b3c130_provenance
a
np:Provenance
.
dgn-np:NP631470.RA5GKlp6nZmrz9gsaLaMgzESnxOoQyZ4LX9FeN03d6b3c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP631470.RA5GKlp6nZmrz9gsaLaMgzESnxOoQyZ4LX9FeN03d6b3c130_assertion
{
miriam-gene:5649
a
ncit:C16612
.
lld:C0013080
a
ncit:C7057
.
dgn-gda:DGNf9719b3fea85aeb9e5a94cb3140d4cfd
sio:SIO_000628
miriam-gene:5649
,
lld:C0013080
;
a
sio:SIO_001121
.
}
dgn-np:NP631470.RA5GKlp6nZmrz9gsaLaMgzESnxOoQyZ4LX9FeN03d6b3c130_provenance
{
dgn-np:NP631470.RA5GKlp6nZmrz9gsaLaMgzESnxOoQyZ4LX9FeN03d6b3c130_assertion
dcterms:description
"[Here we demonstrate pronounced Reelin changes at protein and mRNA levels in the frontal cortex in adult Down's syndrome (DS), where the extra copy of chromosome 21 leads to overexpression of beta-amyloid.]. 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:20025970
;
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:NP631470.RA5GKlp6nZmrz9gsaLaMgzESnxOoQyZ4LX9FeN03d6b3c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:21+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" .
}