@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP467870.RAv3aYvo7SFvMS3454464RW73WQNBy1Y0Nm4de3ABv7A8
> .
@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:NP467870.RAv3aYvo7SFvMS3454464RW73WQNBy1Y0Nm4de3ABv7A8130_head
{
this:
np:hasAssertion
dgn-np:NP467870.RAv3aYvo7SFvMS3454464RW73WQNBy1Y0Nm4de3ABv7A8130_assertion
;
np:hasProvenance
dgn-np:NP467870.RAv3aYvo7SFvMS3454464RW73WQNBy1Y0Nm4de3ABv7A8130_provenance
;
np:hasPublicationInfo
dgn-np:NP467870.RAv3aYvo7SFvMS3454464RW73WQNBy1Y0Nm4de3ABv7A8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP467870.RAv3aYvo7SFvMS3454464RW73WQNBy1Y0Nm4de3ABv7A8130_assertion
a
np:Assertion
.
dgn-np:NP467870.RAv3aYvo7SFvMS3454464RW73WQNBy1Y0Nm4de3ABv7A8130_provenance
a
np:Provenance
.
dgn-np:NP467870.RAv3aYvo7SFvMS3454464RW73WQNBy1Y0Nm4de3ABv7A8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP467870.RAv3aYvo7SFvMS3454464RW73WQNBy1Y0Nm4de3ABv7A8130_assertion
{
miriam-gene:5663
a
ncit:C16612
.
lld:C0233794
a
ncit:C7057
.
dgn-gda:DGN28e8ee03acf6f83f9df1215889b34a00
sio:SIO_000628
miriam-gene:5663
,
lld:C0233794
;
a
sio:SIO_001121
.
}
dgn-np:NP467870.RAv3aYvo7SFvMS3454464RW73WQNBy1Y0Nm4de3ABv7A8130_provenance
{
dgn-np:NP467870.RAv3aYvo7SFvMS3454464RW73WQNBy1Y0Nm4de3ABv7A8130_assertion
dcterms:description
"[These results suggest that the sensorimotor gating is impaired with the progressing of AD phenotype, and its deficit may be correlated to cerebral Aβ neuropathology and memory impairment in the APP/PS1 transgenic mouse model of AD.]. 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:22595040
;
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:NP467870.RAv3aYvo7SFvMS3454464RW73WQNBy1Y0Nm4de3ABv7A8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:40+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" .
}