@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP240332.RAM-Wf15UrAsii7SrraEz7LphMi3yvC43Schiv-8otRBM
> .
@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:NP240332.RAM-Wf15UrAsii7SrraEz7LphMi3yvC43Schiv-8otRBM130_head
{
this:
np:hasAssertion
dgn-np:NP240332.RAM-Wf15UrAsii7SrraEz7LphMi3yvC43Schiv-8otRBM130_assertion
;
np:hasProvenance
dgn-np:NP240332.RAM-Wf15UrAsii7SrraEz7LphMi3yvC43Schiv-8otRBM130_provenance
;
np:hasPublicationInfo
dgn-np:NP240332.RAM-Wf15UrAsii7SrraEz7LphMi3yvC43Schiv-8otRBM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP240332.RAM-Wf15UrAsii7SrraEz7LphMi3yvC43Schiv-8otRBM130_assertion
a
np:Assertion
.
dgn-np:NP240332.RAM-Wf15UrAsii7SrraEz7LphMi3yvC43Schiv-8otRBM130_provenance
a
np:Provenance
.
dgn-np:NP240332.RAM-Wf15UrAsii7SrraEz7LphMi3yvC43Schiv-8otRBM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP240332.RAM-Wf15UrAsii7SrraEz7LphMi3yvC43Schiv-8otRBM130_assertion
{
miriam-gene:472
a
ncit:C16612
.
lld:C0751956
a
ncit:C7057
.
dgn-gda:DGN3b4f0d62002aae095aefabbff8d8b675
sio:SIO_000628
miriam-gene:472
,
lld:C0751956
;
a
sio:SIO_001121
.
}
dgn-np:NP240332.RAM-Wf15UrAsii7SrraEz7LphMi3yvC43Schiv-8otRBM130_provenance
{
dgn-np:NP240332.RAM-Wf15UrAsii7SrraEz7LphMi3yvC43Schiv-8otRBM130_assertion
dcterms:description
"[This study was performed in acute stroke patients in the Turkish population to determine the frequency of the A1166C polymorphism in the AT1 gene and to examine the role of this polymorphism in acute stroke development.]. 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:23480670
;
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:NP240332.RAM-Wf15UrAsii7SrraEz7LphMi3yvC43Schiv-8otRBM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:14+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" .
}