@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP810005.RAZp3QQW6pkj3fmytBUQLtHQnZeqkZXv5s_Um7BmrTnfA
> .
@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:NP810005.RAZp3QQW6pkj3fmytBUQLtHQnZeqkZXv5s_Um7BmrTnfA130_head
{
this:
np:hasAssertion
dgn-np:NP810005.RAZp3QQW6pkj3fmytBUQLtHQnZeqkZXv5s_Um7BmrTnfA130_assertion
;
np:hasProvenance
dgn-np:NP810005.RAZp3QQW6pkj3fmytBUQLtHQnZeqkZXv5s_Um7BmrTnfA130_provenance
;
np:hasPublicationInfo
dgn-np:NP810005.RAZp3QQW6pkj3fmytBUQLtHQnZeqkZXv5s_Um7BmrTnfA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP810005.RAZp3QQW6pkj3fmytBUQLtHQnZeqkZXv5s_Um7BmrTnfA130_assertion
a
np:Assertion
.
dgn-np:NP810005.RAZp3QQW6pkj3fmytBUQLtHQnZeqkZXv5s_Um7BmrTnfA130_provenance
a
np:Provenance
.
dgn-np:NP810005.RAZp3QQW6pkj3fmytBUQLtHQnZeqkZXv5s_Um7BmrTnfA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP810005.RAZp3QQW6pkj3fmytBUQLtHQnZeqkZXv5s_Um7BmrTnfA130_assertion
{
miriam-gene:23621
a
ncit:C16612
.
lld:C0233794
a
ncit:C7057
.
dgn-gda:DGNcd8d477591c861b7fdca236dca3dfb27
sio:SIO_000628
miriam-gene:23621
,
lld:C0233794
;
a
sio:SIO_001121
.
}
dgn-np:NP810005.RAZp3QQW6pkj3fmytBUQLtHQnZeqkZXv5s_Um7BmrTnfA130_provenance
{
dgn-np:NP810005.RAZp3QQW6pkj3fmytBUQLtHQnZeqkZXv5s_Um7BmrTnfA130_assertion
dcterms:description
"[In Tg2576 mice, knockdown by short hairpin RNA or knockout of the S100a9 gene significantly reduced the neuropathology, greatly improved the learning and memory impairment and reduced the amount of Aβ and APP-CTs by increasing neprilysin and decreasing BACE activity.]. 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:22301734
;
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:NP810005.RAZp3QQW6pkj3fmytBUQLtHQnZeqkZXv5s_Um7BmrTnfA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:16+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" .
}