@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP579049.RAKnQaPFntNjTEOiq3ODiTFRoO4KkmcG4ZMPN6kbci-s4
> .
@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:NP579049.RAKnQaPFntNjTEOiq3ODiTFRoO4KkmcG4ZMPN6kbci-s4130_head
{
this:
np:hasAssertion
dgn-np:NP579049.RAKnQaPFntNjTEOiq3ODiTFRoO4KkmcG4ZMPN6kbci-s4130_assertion
;
np:hasProvenance
dgn-np:NP579049.RAKnQaPFntNjTEOiq3ODiTFRoO4KkmcG4ZMPN6kbci-s4130_provenance
;
np:hasPublicationInfo
dgn-np:NP579049.RAKnQaPFntNjTEOiq3ODiTFRoO4KkmcG4ZMPN6kbci-s4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP579049.RAKnQaPFntNjTEOiq3ODiTFRoO4KkmcG4ZMPN6kbci-s4130_assertion
a
np:Assertion
.
dgn-np:NP579049.RAKnQaPFntNjTEOiq3ODiTFRoO4KkmcG4ZMPN6kbci-s4130_provenance
a
np:Provenance
.
dgn-np:NP579049.RAKnQaPFntNjTEOiq3ODiTFRoO4KkmcG4ZMPN6kbci-s4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP579049.RAKnQaPFntNjTEOiq3ODiTFRoO4KkmcG4ZMPN6kbci-s4130_assertion
{
miriam-gene:4976
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN0f95e092f78c68e934c1655e8971353e
sio:SIO_000628
miriam-gene:4976
,
lld:C0020538
;
a
sio:SIO_001121
.
}
dgn-np:NP579049.RAKnQaPFntNjTEOiq3ODiTFRoO4KkmcG4ZMPN6kbci-s4130_provenance
{
dgn-np:NP579049.RAKnQaPFntNjTEOiq3ODiTFRoO4KkmcG4ZMPN6kbci-s4130_assertion
dcterms:description
"[However, the age group analysis in the 40s, 50s, and 60s age subgroups revealed that 15 SNPs out of 26 SNPs genotyped in the OPA1 gene were significantly associated with BP and/or hypertension in the 60s age subgroup and their association P values satisfied the Bonferroni-corrected significance level (P < 0.00625).]. 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:21796221
;
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:NP579049.RAKnQaPFntNjTEOiq3ODiTFRoO4KkmcG4ZMPN6kbci-s4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:49+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" .
}