@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP500817.RA2hh6zCtSN5LWU2snZGiTA9FYLFQpAJ7Sj2WtjhMIbn0
> .
@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:NP500817.RA2hh6zCtSN5LWU2snZGiTA9FYLFQpAJ7Sj2WtjhMIbn0130_head
{
this:
np:hasAssertion
dgn-np:NP500817.RA2hh6zCtSN5LWU2snZGiTA9FYLFQpAJ7Sj2WtjhMIbn0130_assertion
;
np:hasProvenance
dgn-np:NP500817.RA2hh6zCtSN5LWU2snZGiTA9FYLFQpAJ7Sj2WtjhMIbn0130_provenance
;
np:hasPublicationInfo
dgn-np:NP500817.RA2hh6zCtSN5LWU2snZGiTA9FYLFQpAJ7Sj2WtjhMIbn0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP500817.RA2hh6zCtSN5LWU2snZGiTA9FYLFQpAJ7Sj2WtjhMIbn0130_assertion
a
np:Assertion
.
dgn-np:NP500817.RA2hh6zCtSN5LWU2snZGiTA9FYLFQpAJ7Sj2WtjhMIbn0130_provenance
a
np:Provenance
.
dgn-np:NP500817.RA2hh6zCtSN5LWU2snZGiTA9FYLFQpAJ7Sj2WtjhMIbn0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP500817.RA2hh6zCtSN5LWU2snZGiTA9FYLFQpAJ7Sj2WtjhMIbn0130_assertion
{
miriam-gene:9446
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGN09dd22606767f14d2f3f2e71ad314797
sio:SIO_000628
miriam-gene:9446
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP500817.RA2hh6zCtSN5LWU2snZGiTA9FYLFQpAJ7Sj2WtjhMIbn0130_provenance
{
dgn-np:NP500817.RA2hh6zCtSN5LWU2snZGiTA9FYLFQpAJ7Sj2WtjhMIbn0130_assertion
dcterms:description
"[Our findings supported a role of the GSTO1 rs4925 SNP in the risk of sporadic AD in southern Italy, suggesting that this and other variants of the GSTO1 gene could be implicated in AD pathogenesis.]. 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:20818931
;
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:NP500817.RA2hh6zCtSN5LWU2snZGiTA9FYLFQpAJ7Sj2WtjhMIbn0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:58+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" .
}