@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP316376.RAAmi1WMBGLcTEAvZXrsxiMuLKMK6Lx6JMKrVXxpJ-nbE
> .
@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:NP316376.RAAmi1WMBGLcTEAvZXrsxiMuLKMK6Lx6JMKrVXxpJ-nbE130_head
{
this:
np:hasAssertion
dgn-np:NP316376.RAAmi1WMBGLcTEAvZXrsxiMuLKMK6Lx6JMKrVXxpJ-nbE130_assertion
;
np:hasProvenance
dgn-np:NP316376.RAAmi1WMBGLcTEAvZXrsxiMuLKMK6Lx6JMKrVXxpJ-nbE130_provenance
;
np:hasPublicationInfo
dgn-np:NP316376.RAAmi1WMBGLcTEAvZXrsxiMuLKMK6Lx6JMKrVXxpJ-nbE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP316376.RAAmi1WMBGLcTEAvZXrsxiMuLKMK6Lx6JMKrVXxpJ-nbE130_assertion
a
np:Assertion
.
dgn-np:NP316376.RAAmi1WMBGLcTEAvZXrsxiMuLKMK6Lx6JMKrVXxpJ-nbE130_provenance
a
np:Provenance
.
dgn-np:NP316376.RAAmi1WMBGLcTEAvZXrsxiMuLKMK6Lx6JMKrVXxpJ-nbE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP316376.RAAmi1WMBGLcTEAvZXrsxiMuLKMK6Lx6JMKrVXxpJ-nbE130_assertion
{
miriam-gene:72
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGNa50360be5bdcaaaf7790c2bdc2c2c92d
sio:SIO_000628
miriam-gene:72
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP316376.RAAmi1WMBGLcTEAvZXrsxiMuLKMK6Lx6JMKrVXxpJ-nbE130_provenance
{
dgn-np:NP316376.RAAmi1WMBGLcTEAvZXrsxiMuLKMK6Lx6JMKrVXxpJ-nbE130_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:NP316376.RAAmi1WMBGLcTEAvZXrsxiMuLKMK6Lx6JMKrVXxpJ-nbE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:01+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" .
}