@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP165697.RAVHb9l0l3FN6ZH7kkdxiMmUb7wwElqXob9zcZSzZqOvM
> .
@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:NP165697.RAVHb9l0l3FN6ZH7kkdxiMmUb7wwElqXob9zcZSzZqOvM130_head
{
this:
np:hasAssertion
dgn-np:NP165697.RAVHb9l0l3FN6ZH7kkdxiMmUb7wwElqXob9zcZSzZqOvM130_assertion
;
np:hasProvenance
dgn-np:NP165697.RAVHb9l0l3FN6ZH7kkdxiMmUb7wwElqXob9zcZSzZqOvM130_provenance
;
np:hasPublicationInfo
dgn-np:NP165697.RAVHb9l0l3FN6ZH7kkdxiMmUb7wwElqXob9zcZSzZqOvM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP165697.RAVHb9l0l3FN6ZH7kkdxiMmUb7wwElqXob9zcZSzZqOvM130_assertion
a
np:Assertion
.
dgn-np:NP165697.RAVHb9l0l3FN6ZH7kkdxiMmUb7wwElqXob9zcZSzZqOvM130_provenance
a
np:Provenance
.
dgn-np:NP165697.RAVHb9l0l3FN6ZH7kkdxiMmUb7wwElqXob9zcZSzZqOvM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP165697.RAVHb9l0l3FN6ZH7kkdxiMmUb7wwElqXob9zcZSzZqOvM130_assertion
{
miriam-gene:183
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN5e64ba5b1f9a190524a3edea8f3c26de
sio:SIO_000628
miriam-gene:183
,
lld:C0020538
;
a
sio:SIO_001121
.
}
dgn-np:NP165697.RAVHb9l0l3FN6ZH7kkdxiMmUb7wwElqXob9zcZSzZqOvM130_provenance
{
dgn-np:NP165697.RAVHb9l0l3FN6ZH7kkdxiMmUb7wwElqXob9zcZSzZqOvM130_assertion
dcterms:description
"[We carried out association studies and multivariate analyses including other candidate causal factors of HP such as the M235T variant of the angiotensinogen (AGT) gene, prepregnancy body mass index (BMI), and family history of hypertension in Japanese 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:15042429
;
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:NP165697.RAVHb9l0l3FN6ZH7kkdxiMmUb7wwElqXob9zcZSzZqOvM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:29+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" .
}