@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP44703.RAUSz9cMoHTeTihGa0SE8NhGOBD1M9Y-4_ovL8BOG-1yY
> .
@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:NP44703.RAUSz9cMoHTeTihGa0SE8NhGOBD1M9Y-4_ovL8BOG-1yY130_head
{
this:
np:hasAssertion
dgn-np:NP44703.RAUSz9cMoHTeTihGa0SE8NhGOBD1M9Y-4_ovL8BOG-1yY130_assertion
;
np:hasProvenance
dgn-np:NP44703.RAUSz9cMoHTeTihGa0SE8NhGOBD1M9Y-4_ovL8BOG-1yY130_provenance
;
np:hasPublicationInfo
dgn-np:NP44703.RAUSz9cMoHTeTihGa0SE8NhGOBD1M9Y-4_ovL8BOG-1yY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP44703.RAUSz9cMoHTeTihGa0SE8NhGOBD1M9Y-4_ovL8BOG-1yY130_assertion
a
np:Assertion
.
dgn-np:NP44703.RAUSz9cMoHTeTihGa0SE8NhGOBD1M9Y-4_ovL8BOG-1yY130_provenance
a
np:Provenance
.
dgn-np:NP44703.RAUSz9cMoHTeTihGa0SE8NhGOBD1M9Y-4_ovL8BOG-1yY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP44703.RAUSz9cMoHTeTihGa0SE8NhGOBD1M9Y-4_ovL8BOG-1yY130_assertion
{
miriam-gene:2099
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGNa450aee5942d2700b8017f9673f6ebda
sio:SIO_000628
miriam-gene:2099
,
lld:C0002395
;
a
sio:SIO_001122
.
}
dgn-np:NP44703.RAUSz9cMoHTeTihGa0SE8NhGOBD1M9Y-4_ovL8BOG-1yY130_provenance
{
dgn-np:NP44703.RAUSz9cMoHTeTihGa0SE8NhGOBD1M9Y-4_ovL8BOG-1yY130_assertion
dcterms:description
"[In this study, 16 single nucleotide polymorphisms (SNPs) of the ESR1 gene (including four commonly studied ESR1 SNPs and 12 other tagging SNPs selected from the HapMap database) were investigated to further evaluate the association between ESR1 polymorphisms and the risk of AD in the Chinese population.]. 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:19586561
;
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:NP44703.RAUSz9cMoHTeTihGa0SE8NhGOBD1M9Y-4_ovL8BOG-1yY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:20+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" .
}