@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP685795.RAO6kN426_rpE3kBRQEQl9hQDbv2AqMyRDRZRf454eGXw
> .
@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:NP685795.RAO6kN426_rpE3kBRQEQl9hQDbv2AqMyRDRZRf454eGXw130_head
{
this:
np:hasAssertion
dgn-np:NP685795.RAO6kN426_rpE3kBRQEQl9hQDbv2AqMyRDRZRf454eGXw130_assertion
;
np:hasProvenance
dgn-np:NP685795.RAO6kN426_rpE3kBRQEQl9hQDbv2AqMyRDRZRf454eGXw130_provenance
;
np:hasPublicationInfo
dgn-np:NP685795.RAO6kN426_rpE3kBRQEQl9hQDbv2AqMyRDRZRf454eGXw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP685795.RAO6kN426_rpE3kBRQEQl9hQDbv2AqMyRDRZRf454eGXw130_assertion
a
np:Assertion
.
dgn-np:NP685795.RAO6kN426_rpE3kBRQEQl9hQDbv2AqMyRDRZRf454eGXw130_provenance
a
np:Provenance
.
dgn-np:NP685795.RAO6kN426_rpE3kBRQEQl9hQDbv2AqMyRDRZRf454eGXw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP685795.RAO6kN426_rpE3kBRQEQl9hQDbv2AqMyRDRZRf454eGXw130_assertion
{
miriam-gene:23336
a
ncit:C16612
.
lld:C0001614
a
ncit:C7057
.
dgn-gda:DGNa087d4c12079ad5fd47021a6eeaef644
sio:SIO_000628
miriam-gene:23336
,
lld:C0001614
;
a
sio:SIO_001121
.
}
dgn-np:NP685795.RAO6kN426_rpE3kBRQEQl9hQDbv2AqMyRDRZRf454eGXw130_provenance
{
dgn-np:NP685795.RAO6kN426_rpE3kBRQEQl9hQDbv2AqMyRDRZRf454eGXw130_assertion
dcterms:description
"[Furthermore, function-based functional connectivities (FCs) in the region of interesting (ROI) (posterior cingulate cortex (PCC) of the DMN) were analysed to explore interactions between disease states, task states and genetic risk factors (APOE4).]. 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:23270974
;
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:NP685795.RAO6kN426_rpE3kBRQEQl9hQDbv2AqMyRDRZRf454eGXw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:57+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" .
}