@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP298768.RAjwrxz4Rit4wuZgONLl0HSYyE1KB4O-hC2eVVJar6RZg
> .
@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:NP298768.RAjwrxz4Rit4wuZgONLl0HSYyE1KB4O-hC2eVVJar6RZg130_head
{
this:
np:hasAssertion
dgn-np:NP298768.RAjwrxz4Rit4wuZgONLl0HSYyE1KB4O-hC2eVVJar6RZg130_assertion
;
np:hasProvenance
dgn-np:NP298768.RAjwrxz4Rit4wuZgONLl0HSYyE1KB4O-hC2eVVJar6RZg130_provenance
;
np:hasPublicationInfo
dgn-np:NP298768.RAjwrxz4Rit4wuZgONLl0HSYyE1KB4O-hC2eVVJar6RZg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP298768.RAjwrxz4Rit4wuZgONLl0HSYyE1KB4O-hC2eVVJar6RZg130_assertion
a
np:Assertion
.
dgn-np:NP298768.RAjwrxz4Rit4wuZgONLl0HSYyE1KB4O-hC2eVVJar6RZg130_provenance
a
np:Provenance
.
dgn-np:NP298768.RAjwrxz4Rit4wuZgONLl0HSYyE1KB4O-hC2eVVJar6RZg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP298768.RAjwrxz4Rit4wuZgONLl0HSYyE1KB4O-hC2eVVJar6RZg130_assertion
{
miriam-gene:3596
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGN083c8026eb7343de37b5ca40e05c66c8
sio:SIO_000628
miriam-gene:3596
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP298768.RAjwrxz4Rit4wuZgONLl0HSYyE1KB4O-hC2eVVJar6RZg130_provenance
{
dgn-np:NP298768.RAjwrxz4Rit4wuZgONLl0HSYyE1KB4O-hC2eVVJar6RZg130_assertion
dcterms:description
"[Their more severe reduction in N400 repetition effect, than P600, is in contrast to the reverse pattern reported in amnestic mild cognitive impairment and incipient Alzheimer's disease (Olichney et al., 2008).]. 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:20410144
;
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:NP298768.RAjwrxz4Rit4wuZgONLl0HSYyE1KB4O-hC2eVVJar6RZg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:49+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" .
}