@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP722434.RAI8pcjRg-PlmjSHAewdocyQR4qEa44lL1u9lJ60VXRJA
> .
@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:NP722434.RAI8pcjRg-PlmjSHAewdocyQR4qEa44lL1u9lJ60VXRJA130_head
{
this:
np:hasAssertion
dgn-np:NP722434.RAI8pcjRg-PlmjSHAewdocyQR4qEa44lL1u9lJ60VXRJA130_assertion
;
np:hasProvenance
dgn-np:NP722434.RAI8pcjRg-PlmjSHAewdocyQR4qEa44lL1u9lJ60VXRJA130_provenance
;
np:hasPublicationInfo
dgn-np:NP722434.RAI8pcjRg-PlmjSHAewdocyQR4qEa44lL1u9lJ60VXRJA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP722434.RAI8pcjRg-PlmjSHAewdocyQR4qEa44lL1u9lJ60VXRJA130_assertion
a
np:Assertion
.
dgn-np:NP722434.RAI8pcjRg-PlmjSHAewdocyQR4qEa44lL1u9lJ60VXRJA130_provenance
a
np:Provenance
.
dgn-np:NP722434.RAI8pcjRg-PlmjSHAewdocyQR4qEa44lL1u9lJ60VXRJA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP722434.RAI8pcjRg-PlmjSHAewdocyQR4qEa44lL1u9lJ60VXRJA130_assertion
{
miriam-gene:11332
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGN79dfc48fb47af4d67bf51b817b847408
sio:SIO_000628
miriam-gene:11332
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP722434.RAI8pcjRg-PlmjSHAewdocyQR4qEa44lL1u9lJ60VXRJA130_provenance
{
dgn-np:NP722434.RAI8pcjRg-PlmjSHAewdocyQR4qEa44lL1u9lJ60VXRJA130_assertion
dcterms:description
"[Our data failed to detect any effect of polymorphism in the ACT genotypes associated with the APOE alleles, suggesting that in this population ACT does not increase the risk of AD.]. 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:9280167
;
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:NP722434.RAI8pcjRg-PlmjSHAewdocyQR4qEa44lL1u9lJ60VXRJA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:18+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" .
}