@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP88242.RAo8bIMMgQ_0Dr65Ud3hNERIysvfCPxt6GejHDT1b5hcw
> .
@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:NP88242.RAo8bIMMgQ_0Dr65Ud3hNERIysvfCPxt6GejHDT1b5hcw130_head
{
this:
np:hasAssertion
dgn-np:NP88242.RAo8bIMMgQ_0Dr65Ud3hNERIysvfCPxt6GejHDT1b5hcw130_assertion
;
np:hasProvenance
dgn-np:NP88242.RAo8bIMMgQ_0Dr65Ud3hNERIysvfCPxt6GejHDT1b5hcw130_provenance
;
np:hasPublicationInfo
dgn-np:NP88242.RAo8bIMMgQ_0Dr65Ud3hNERIysvfCPxt6GejHDT1b5hcw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP88242.RAo8bIMMgQ_0Dr65Ud3hNERIysvfCPxt6GejHDT1b5hcw130_assertion
a
np:Assertion
.
dgn-np:NP88242.RAo8bIMMgQ_0Dr65Ud3hNERIysvfCPxt6GejHDT1b5hcw130_provenance
a
np:Provenance
.
dgn-np:NP88242.RAo8bIMMgQ_0Dr65Ud3hNERIysvfCPxt6GejHDT1b5hcw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP88242.RAo8bIMMgQ_0Dr65Ud3hNERIysvfCPxt6GejHDT1b5hcw130_assertion
{
miriam-gene:2100
a
ncit:C16612
.
lld:C0338656
a
ncit:C7057
.
dgn-gda:DGN65e264fa1ced1d94166b9dde8ad0e242
sio:SIO_000628
miriam-gene:2100
,
lld:C0338656
;
a
sio:SIO_001122
.
}
dgn-np:NP88242.RAo8bIMMgQ_0Dr65Ud3hNERIysvfCPxt6GejHDT1b5hcw130_provenance
{
dgn-np:NP88242.RAo8bIMMgQ_0Dr65Ud3hNERIysvfCPxt6GejHDT1b5hcw130_assertion
dcterms:description
"[Among women, after multivariate adjustment, two of the ESR1 SNPs (rs8179176, rs9340799) and two of the ESR2 SNPs (rs1256065, rs1256030) were associated with likelihood of developing cognitive impairment, although the association for rs8179176 was of trend level significance.]. 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:17889406
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP88242.RAo8bIMMgQ_0Dr65Ud3hNERIysvfCPxt6GejHDT1b5hcw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:43+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" .
}