@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP548894.RAU4qBeUIOoplu8yAGgoRvkgzIOaUgenqEcN-ZbbIcZpg
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP548894.RAU4qBeUIOoplu8yAGgoRvkgzIOaUgenqEcN-ZbbIcZpg130_head
{
this:
np:hasAssertion
dgn-np:NP548894.RAU4qBeUIOoplu8yAGgoRvkgzIOaUgenqEcN-ZbbIcZpg130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP548894.RAU4qBeUIOoplu8yAGgoRvkgzIOaUgenqEcN-ZbbIcZpg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP548894.RAU4qBeUIOoplu8yAGgoRvkgzIOaUgenqEcN-ZbbIcZpg130_assertion
a
np:Assertion
.
dgn-np:NP548894.RAU4qBeUIOoplu8yAGgoRvkgzIOaUgenqEcN-ZbbIcZpg130_provenance
a
np:Provenance
.
dgn-np:NP548894.RAU4qBeUIOoplu8yAGgoRvkgzIOaUgenqEcN-ZbbIcZpg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP548894.RAU4qBeUIOoplu8yAGgoRvkgzIOaUgenqEcN-ZbbIcZpg130_assertion
{
miriam-gene:146
a
ncit:C16612
.
lld:C0085580
a
ncit:C7057
.
dgn-gda:DGNda165c0c4b6d75118c917a218be0a711
sio:SIO_000628
miriam-gene:146
,
lld:C0085580
;
a
sio:SIO_001121
.
}
dgn-np:NP548894.RAU4qBeUIOoplu8yAGgoRvkgzIOaUgenqEcN-ZbbIcZpg130_provenance
{
dgn-np:NP548894.RAU4qBeUIOoplu8yAGgoRvkgzIOaUgenqEcN-ZbbIcZpg130_assertion
dcterms:description
"[Our findings suggest that the genetic variations in the ADRA1A gene are significantly associated with essential hypertension, and may play an important role in the development of essential hypertension in this Chinese population.]. 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:16685204
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP548894.RAU4qBeUIOoplu8yAGgoRvkgzIOaUgenqEcN-ZbbIcZpg130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:53+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}