@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1060357.RA7Xu7WVsjGG84oh8kvF6Xufu3yHKF6g2PkZS1jQ8ZdYo
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1060357.RA7Xu7WVsjGG84oh8kvF6Xufu3yHKF6g2PkZS1jQ8ZdYo130_head
{
this:
np:hasAssertion
dgn-np:NP1060357.RA7Xu7WVsjGG84oh8kvF6Xufu3yHKF6g2PkZS1jQ8ZdYo130_assertion
;
np:hasProvenance
dgn-np:NP1060357.RA7Xu7WVsjGG84oh8kvF6Xufu3yHKF6g2PkZS1jQ8ZdYo130_provenance
;
np:hasPublicationInfo
dgn-np:NP1060357.RA7Xu7WVsjGG84oh8kvF6Xufu3yHKF6g2PkZS1jQ8ZdYo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1060357.RA7Xu7WVsjGG84oh8kvF6Xufu3yHKF6g2PkZS1jQ8ZdYo130_assertion
a
np:Assertion
.
dgn-np:NP1060357.RA7Xu7WVsjGG84oh8kvF6Xufu3yHKF6g2PkZS1jQ8ZdYo130_provenance
a
np:Provenance
.
dgn-np:NP1060357.RA7Xu7WVsjGG84oh8kvF6Xufu3yHKF6g2PkZS1jQ8ZdYo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1060357.RA7Xu7WVsjGG84oh8kvF6Xufu3yHKF6g2PkZS1jQ8ZdYo130_assertion
{
miriam-gene:2100
a
ncit:C16612
.
lld:C0011265
a
ncit:C7057
.
dgn-gda:DGN5f83cf7f977741a2399b2b40ce13e2a6
sio:SIO_000628
miriam-gene:2100
,
lld:C0011265
;
a
sio:SIO_001121
.
}
dgn-np:NP1060357.RA7Xu7WVsjGG84oh8kvF6Xufu3yHKF6g2PkZS1jQ8ZdYo130_provenance
{
dgn-np:NP1060357.RA7Xu7WVsjGG84oh8kvF6Xufu3yHKF6g2PkZS1jQ8ZdYo130_assertion
dcterms:description
"[Although there was only weak support for a gender-specific association between the common ESR1rs2234693 polymorphism and AD, this polymorphism may act as an effect modifier, modifying the association between an ESR2 polymorphism and dementia, as well as the risk of AD associated with the APOE ε4 allele.]. 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:23491264
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1060357.RA7Xu7WVsjGG84oh8kvF6Xufu3yHKF6g2PkZS1jQ8ZdYo130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:47+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}