@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP637918.RAd19_A0mhHino3eRpawhmSHYcWJVsB9Hp8nVVDEfjUvQ
> .
@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:NP637918.RAd19_A0mhHino3eRpawhmSHYcWJVsB9Hp8nVVDEfjUvQ130_head
{
this:
np:hasAssertion
dgn-np:NP637918.RAd19_A0mhHino3eRpawhmSHYcWJVsB9Hp8nVVDEfjUvQ130_assertion
;
np:hasProvenance
dgn-np:NP637918.RAd19_A0mhHino3eRpawhmSHYcWJVsB9Hp8nVVDEfjUvQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP637918.RAd19_A0mhHino3eRpawhmSHYcWJVsB9Hp8nVVDEfjUvQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP637918.RAd19_A0mhHino3eRpawhmSHYcWJVsB9Hp8nVVDEfjUvQ130_assertion
a
np:Assertion
.
dgn-np:NP637918.RAd19_A0mhHino3eRpawhmSHYcWJVsB9Hp8nVVDEfjUvQ130_provenance
a
np:Provenance
.
dgn-np:NP637918.RAd19_A0mhHino3eRpawhmSHYcWJVsB9Hp8nVVDEfjUvQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP637918.RAd19_A0mhHino3eRpawhmSHYcWJVsB9Hp8nVVDEfjUvQ130_assertion
{
miriam-gene:2099
a
ncit:C16612
.
lld:C0004153
a
ncit:C7057
.
dgn-gda:DGNa94e08626ffc059191ffff2a7adf9a56
sio:SIO_000628
miriam-gene:2099
,
lld:C0004153
;
a
sio:SIO_001121
.
}
dgn-np:NP637918.RAd19_A0mhHino3eRpawhmSHYcWJVsB9Hp8nVVDEfjUvQ130_provenance
{
dgn-np:NP637918.RAd19_A0mhHino3eRpawhmSHYcWJVsB9Hp8nVVDEfjUvQ130_assertion
dcterms:description
"[Since hypertension and atherosclerosis are major mechanisms in stroke development, we hypothesized that genetic variants of the ER alpha gene (ESR1) are determinants of future ischemic stroke or intracerebral hemorrhage (ICH).]. 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:17971628
;
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:NP637918.RAd19_A0mhHino3eRpawhmSHYcWJVsB9Hp8nVVDEfjUvQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:34+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" .
}