@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP594058.RAzhjTC-i3gnpQOQRWda0wQZbqif2JCkfhBLvehW49dtc
> .
@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:NP594058.RAzhjTC-i3gnpQOQRWda0wQZbqif2JCkfhBLvehW49dtc130_head
{
this:
np:hasAssertion
dgn-np:NP594058.RAzhjTC-i3gnpQOQRWda0wQZbqif2JCkfhBLvehW49dtc130_assertion
;
np:hasProvenance
dgn-np:NP594058.RAzhjTC-i3gnpQOQRWda0wQZbqif2JCkfhBLvehW49dtc130_provenance
;
np:hasPublicationInfo
dgn-np:NP594058.RAzhjTC-i3gnpQOQRWda0wQZbqif2JCkfhBLvehW49dtc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP594058.RAzhjTC-i3gnpQOQRWda0wQZbqif2JCkfhBLvehW49dtc130_assertion
a
np:Assertion
.
dgn-np:NP594058.RAzhjTC-i3gnpQOQRWda0wQZbqif2JCkfhBLvehW49dtc130_provenance
a
np:Provenance
.
dgn-np:NP594058.RAzhjTC-i3gnpQOQRWda0wQZbqif2JCkfhBLvehW49dtc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP594058.RAzhjTC-i3gnpQOQRWda0wQZbqif2JCkfhBLvehW49dtc130_assertion
{
miriam-gene:2638
a
ncit:C16612
.
lld:C0038454
a
ncit:C7057
.
dgn-gda:DGNd23256c04cf9807b01d7d2ac7a33fb6c
sio:SIO_000628
miriam-gene:2638
,
lld:C0038454
;
a
sio:SIO_001121
.
}
dgn-np:NP594058.RAzhjTC-i3gnpQOQRWda0wQZbqif2JCkfhBLvehW49dtc130_provenance
{
dgn-np:NP594058.RAzhjTC-i3gnpQOQRWda0wQZbqif2JCkfhBLvehW49dtc130_assertion
dcterms:description
"[Discriminant function tests yielded baseline SBP, DBP, smoking, and parental history of stroke or hypertension to be the most significant precursors distinguishing hypertensive from normotensive groups, and the model correctly classified 69.7% of the subjects.]. 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:4036789
;
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:NP594058.RAzhjTC-i3gnpQOQRWda0wQZbqif2JCkfhBLvehW49dtc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:57+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" .
}