@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP297514.RAmtO-QCflBzClqgCgH1rUS1cbcWRZVipu9YnvKtFv7LY
> .
@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:NP297514.RAmtO-QCflBzClqgCgH1rUS1cbcWRZVipu9YnvKtFv7LY130_head
{
this:
np:hasAssertion
dgn-np:NP297514.RAmtO-QCflBzClqgCgH1rUS1cbcWRZVipu9YnvKtFv7LY130_assertion
;
np:hasProvenance
dgn-np:NP297514.RAmtO-QCflBzClqgCgH1rUS1cbcWRZVipu9YnvKtFv7LY130_provenance
;
np:hasPublicationInfo
dgn-np:NP297514.RAmtO-QCflBzClqgCgH1rUS1cbcWRZVipu9YnvKtFv7LY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP297514.RAmtO-QCflBzClqgCgH1rUS1cbcWRZVipu9YnvKtFv7LY130_assertion
a
np:Assertion
.
dgn-np:NP297514.RAmtO-QCflBzClqgCgH1rUS1cbcWRZVipu9YnvKtFv7LY130_provenance
a
np:Provenance
.
dgn-np:NP297514.RAmtO-QCflBzClqgCgH1rUS1cbcWRZVipu9YnvKtFv7LY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP297514.RAmtO-QCflBzClqgCgH1rUS1cbcWRZVipu9YnvKtFv7LY130_assertion
{
miriam-gene:627
a
ncit:C16612
.
lld:C0001614
a
ncit:C7057
.
dgn-gda:DGN6285ccc374b34c99505877173fe9dd65
sio:SIO_000628
miriam-gene:627
,
lld:C0001614
;
a
sio:SIO_001121
.
}
dgn-np:NP297514.RAmtO-QCflBzClqgCgH1rUS1cbcWRZVipu9YnvKtFv7LY130_provenance
{
dgn-np:NP297514.RAmtO-QCflBzClqgCgH1rUS1cbcWRZVipu9YnvKtFv7LY130_assertion
dcterms:description
"[The BDNF Val66Met polymorphism interacted with age to predict (1) cortical thickness (prominently at the entorhinal cortex and temporal gyri), (2) fractional anisotropy of white matter tracts (prominently at white matter tracts connecting to the medial temporal lobe), and (3) episodic memory performance.]. 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:21300947
;
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:NP297514.RAmtO-QCflBzClqgCgH1rUS1cbcWRZVipu9YnvKtFv7LY130_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" .
}