@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP52101.RA2tSwtxrMgk4nmp7KGufJDrslkWSdibT5VoAlnAf7mJI
> .
@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:NP52101.RA2tSwtxrMgk4nmp7KGufJDrslkWSdibT5VoAlnAf7mJI130_head
{
this:
np:hasAssertion
dgn-np:NP52101.RA2tSwtxrMgk4nmp7KGufJDrslkWSdibT5VoAlnAf7mJI130_assertion
;
np:hasProvenance
dgn-np:NP52101.RA2tSwtxrMgk4nmp7KGufJDrslkWSdibT5VoAlnAf7mJI130_provenance
;
np:hasPublicationInfo
dgn-np:NP52101.RA2tSwtxrMgk4nmp7KGufJDrslkWSdibT5VoAlnAf7mJI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP52101.RA2tSwtxrMgk4nmp7KGufJDrslkWSdibT5VoAlnAf7mJI130_assertion
a
np:Assertion
.
dgn-np:NP52101.RA2tSwtxrMgk4nmp7KGufJDrslkWSdibT5VoAlnAf7mJI130_provenance
a
np:Provenance
.
dgn-np:NP52101.RA2tSwtxrMgk4nmp7KGufJDrslkWSdibT5VoAlnAf7mJI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP52101.RA2tSwtxrMgk4nmp7KGufJDrslkWSdibT5VoAlnAf7mJI130_assertion
{
miriam-gene:6337
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGNadea5133689e38bf2b64ce7b49fa733a
sio:SIO_000628
miriam-gene:6337
,
lld:C0020538
;
a
sio:SIO_001122
.
}
dgn-np:NP52101.RA2tSwtxrMgk4nmp7KGufJDrslkWSdibT5VoAlnAf7mJI130_provenance
{
dgn-np:NP52101.RA2tSwtxrMgk4nmp7KGufJDrslkWSdibT5VoAlnAf7mJI130_assertion
dcterms:description
"[Our data did not support the association between Mendelian disease gene variants and essential hypertension in the Japanese. However, the present study did not definitively resolve this issue and further investigation is certainly warranted.]. 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:11675945
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP52101.RA2tSwtxrMgk4nmp7KGufJDrslkWSdibT5VoAlnAf7mJI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:24+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" .
}