@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP773844.RARu354Vz-N5x4WJSNRCvPktNVmaGNhnQ63L05omrRtSE
> .
@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:NP773844.RARu354Vz-N5x4WJSNRCvPktNVmaGNhnQ63L05omrRtSE130_head
{
this:
np:hasAssertion
dgn-np:NP773844.RARu354Vz-N5x4WJSNRCvPktNVmaGNhnQ63L05omrRtSE130_assertion
;
np:hasProvenance
dgn-np:NP773844.RARu354Vz-N5x4WJSNRCvPktNVmaGNhnQ63L05omrRtSE130_provenance
;
np:hasPublicationInfo
dgn-np:NP773844.RARu354Vz-N5x4WJSNRCvPktNVmaGNhnQ63L05omrRtSE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP773844.RARu354Vz-N5x4WJSNRCvPktNVmaGNhnQ63L05omrRtSE130_assertion
a
np:Assertion
.
dgn-np:NP773844.RARu354Vz-N5x4WJSNRCvPktNVmaGNhnQ63L05omrRtSE130_provenance
a
np:Provenance
.
dgn-np:NP773844.RARu354Vz-N5x4WJSNRCvPktNVmaGNhnQ63L05omrRtSE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP773844.RARu354Vz-N5x4WJSNRCvPktNVmaGNhnQ63L05omrRtSE130_assertion
{
miriam-gene:4846
a
ncit:C16612
.
lld:C0340557
a
ncit:C7057
.
dgn-gda:DGNa1304719ef981ddf5b777e292182cb3d
sio:SIO_000628
miriam-gene:4846
,
lld:C0340557
;
a
sio:SIO_001121
.
}
dgn-np:NP773844.RARu354Vz-N5x4WJSNRCvPktNVmaGNhnQ63L05omrRtSE130_provenance
{
dgn-np:NP773844.RARu354Vz-N5x4WJSNRCvPktNVmaGNhnQ63L05omrRtSE130_assertion
dcterms:description
"[The Asp allele of the eNOS Glu298Asp polymorphism was associated with atherosclerotic renal artery stenosis with an odds ratio of 1.44 (95% confidence interval 1.00 to 2.09) versus hypertensives with angiographically proven patent arteries, of 1.89 (1.24 to 2.87) versus hypertensive family practice controls, and of 2.09 (1.29 to 3.38) versus normotensive family practice controls.]. 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:15326089
;
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:NP773844.RARu354Vz-N5x4WJSNRCvPktNVmaGNhnQ63L05omrRtSE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:48+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" .
}