@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP126734.RAI9YAwrEjEqcJw3ZJCPEAOxlNvCHVPPd1bjaEPaK41sY
> .
@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:NP126734.RAI9YAwrEjEqcJw3ZJCPEAOxlNvCHVPPd1bjaEPaK41sY130_head
{
this:
np:hasAssertion
dgn-np:NP126734.RAI9YAwrEjEqcJw3ZJCPEAOxlNvCHVPPd1bjaEPaK41sY130_assertion
;
np:hasProvenance
dgn-np:NP126734.RAI9YAwrEjEqcJw3ZJCPEAOxlNvCHVPPd1bjaEPaK41sY130_provenance
;
np:hasPublicationInfo
dgn-np:NP126734.RAI9YAwrEjEqcJw3ZJCPEAOxlNvCHVPPd1bjaEPaK41sY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP126734.RAI9YAwrEjEqcJw3ZJCPEAOxlNvCHVPPd1bjaEPaK41sY130_assertion
a
np:Assertion
.
dgn-np:NP126734.RAI9YAwrEjEqcJw3ZJCPEAOxlNvCHVPPd1bjaEPaK41sY130_provenance
a
np:Provenance
.
dgn-np:NP126734.RAI9YAwrEjEqcJw3ZJCPEAOxlNvCHVPPd1bjaEPaK41sY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP126734.RAI9YAwrEjEqcJw3ZJCPEAOxlNvCHVPPd1bjaEPaK41sY130_assertion
{
miriam-gene:351
a
ncit:C16612
.
lld:C0013080
a
ncit:C7057
.
dgn-gda:DGNff245827090a84063cc631030859cb30
sio:SIO_000628
miriam-gene:351
,
lld:C0013080
;
a
sio:SIO_001123
.
}
dgn-np:NP126734.RAI9YAwrEjEqcJw3ZJCPEAOxlNvCHVPPd1bjaEPaK41sY130_provenance
{
dgn-np:NP126734.RAI9YAwrEjEqcJw3ZJCPEAOxlNvCHVPPd1bjaEPaK41sY130_assertion
dcterms:description
"[The increasing levels of Abeta in CSF during early childhood of Down syndrome patients observed in this study are probably due to the trisomy of the Abeta precursor APP, which leads to an overproduction of Abeta.]. 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:17914261
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP126734.RAI9YAwrEjEqcJw3ZJCPEAOxlNvCHVPPd1bjaEPaK41sY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:06+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" .
}