@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP791746.RAFvUdBaQ9_nyoA_rmKTH332BeaOfDAvpJePwCeREzNnI
> .
@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:NP791746.RAFvUdBaQ9_nyoA_rmKTH332BeaOfDAvpJePwCeREzNnI130_head
{
this:
np:hasAssertion
dgn-np:NP791746.RAFvUdBaQ9_nyoA_rmKTH332BeaOfDAvpJePwCeREzNnI130_assertion
;
np:hasProvenance
dgn-np:NP791746.RAFvUdBaQ9_nyoA_rmKTH332BeaOfDAvpJePwCeREzNnI130_provenance
;
np:hasPublicationInfo
dgn-np:NP791746.RAFvUdBaQ9_nyoA_rmKTH332BeaOfDAvpJePwCeREzNnI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP791746.RAFvUdBaQ9_nyoA_rmKTH332BeaOfDAvpJePwCeREzNnI130_assertion
a
np:Assertion
.
dgn-np:NP791746.RAFvUdBaQ9_nyoA_rmKTH332BeaOfDAvpJePwCeREzNnI130_provenance
a
np:Provenance
.
dgn-np:NP791746.RAFvUdBaQ9_nyoA_rmKTH332BeaOfDAvpJePwCeREzNnI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP791746.RAFvUdBaQ9_nyoA_rmKTH332BeaOfDAvpJePwCeREzNnI130_assertion
{
miriam-gene:2057
a
ncit:C16612
.
lld:C0338656
a
ncit:C7057
.
dgn-gda:DGNd3898fceb10cf55de648c82a33f02b3b
sio:SIO_000628
miriam-gene:2057
,
lld:C0338656
;
a
sio:SIO_001121
.
}
dgn-np:NP791746.RAFvUdBaQ9_nyoA_rmKTH332BeaOfDAvpJePwCeREzNnI130_provenance
{
dgn-np:NP791746.RAFvUdBaQ9_nyoA_rmKTH332BeaOfDAvpJePwCeREzNnI130_assertion
dcterms:description
"[We hypothesized that an intrinsic role of EPO for cognition exists, with particular relevance in situations of cognitive decline, which is reflected by associations of EPO and EPO receptor (EPOR) genotypes with cognitive functions.]. 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:22669473
;
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:NP791746.RAFvUdBaQ9_nyoA_rmKTH332BeaOfDAvpJePwCeREzNnI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:06+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" .
}