@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP233404.RAEiGhb_XnvqHW59tMasLOiyB7jAW7-spme7V3jcJ4Y40
> .
@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:NP233404.RAEiGhb_XnvqHW59tMasLOiyB7jAW7-spme7V3jcJ4Y40130_head
{
this:
np:hasAssertion
dgn-np:NP233404.RAEiGhb_XnvqHW59tMasLOiyB7jAW7-spme7V3jcJ4Y40130_assertion
;
np:hasProvenance
dgn-np:NP233404.RAEiGhb_XnvqHW59tMasLOiyB7jAW7-spme7V3jcJ4Y40130_provenance
;
np:hasPublicationInfo
dgn-np:NP233404.RAEiGhb_XnvqHW59tMasLOiyB7jAW7-spme7V3jcJ4Y40130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP233404.RAEiGhb_XnvqHW59tMasLOiyB7jAW7-spme7V3jcJ4Y40130_assertion
a
np:Assertion
.
dgn-np:NP233404.RAEiGhb_XnvqHW59tMasLOiyB7jAW7-spme7V3jcJ4Y40130_provenance
a
np:Provenance
.
dgn-np:NP233404.RAEiGhb_XnvqHW59tMasLOiyB7jAW7-spme7V3jcJ4Y40130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP233404.RAEiGhb_XnvqHW59tMasLOiyB7jAW7-spme7V3jcJ4Y40130_assertion
{
miriam-gene:345643
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGNee293c7e08c4d7de1666eb24b7817b69
sio:SIO_000628
miriam-gene:345643
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP233404.RAEiGhb_XnvqHW59tMasLOiyB7jAW7-spme7V3jcJ4Y40130_provenance
{
dgn-np:NP233404.RAEiGhb_XnvqHW59tMasLOiyB7jAW7-spme7V3jcJ4Y40130_assertion
dcterms:description
"[Individuals at genetic risk for AD by virtue of the APOE ε4 allele demonstrated increased MTL resting state CBF relative to ε4 noncarriers, whereas individuals characterized as MCI showed decreased MTL resting state CBF relative to their cognitively normal peers.]. 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:22531427
;
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:NP233404.RAEiGhb_XnvqHW59tMasLOiyB7jAW7-spme7V3jcJ4Y40130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:11+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" .
}