@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP49163.RA7z6r60sDoI3XDu3qKqy95wIdFHJ7_d1uj_zNLRbqf48
> .
@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:NP49163.RA7z6r60sDoI3XDu3qKqy95wIdFHJ7_d1uj_zNLRbqf48130_head
{
this:
np:hasAssertion
dgn-np:NP49163.RA7z6r60sDoI3XDu3qKqy95wIdFHJ7_d1uj_zNLRbqf48130_assertion
;
np:hasProvenance
dgn-np:NP49163.RA7z6r60sDoI3XDu3qKqy95wIdFHJ7_d1uj_zNLRbqf48130_provenance
;
np:hasPublicationInfo
dgn-np:NP49163.RA7z6r60sDoI3XDu3qKqy95wIdFHJ7_d1uj_zNLRbqf48130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP49163.RA7z6r60sDoI3XDu3qKqy95wIdFHJ7_d1uj_zNLRbqf48130_assertion
a
np:Assertion
.
dgn-np:NP49163.RA7z6r60sDoI3XDu3qKqy95wIdFHJ7_d1uj_zNLRbqf48130_provenance
a
np:Provenance
.
dgn-np:NP49163.RA7z6r60sDoI3XDu3qKqy95wIdFHJ7_d1uj_zNLRbqf48130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP49163.RA7z6r60sDoI3XDu3qKqy95wIdFHJ7_d1uj_zNLRbqf48130_assertion
{
miriam-gene:148
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN11ef17f456ed0c94fd76ada729d0cf0f
sio:SIO_000628
miriam-gene:148
,
lld:C0020538
;
a
sio:SIO_001122
.
}
dgn-np:NP49163.RA7z6r60sDoI3XDu3qKqy95wIdFHJ7_d1uj_zNLRbqf48130_provenance
{
dgn-np:NP49163.RA7z6r60sDoI3XDu3qKqy95wIdFHJ7_d1uj_zNLRbqf48130_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: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:NP49163.RA7z6r60sDoI3XDu3qKqy95wIdFHJ7_d1uj_zNLRbqf48130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:22+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" .
}