@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP247809.RATVeApVNcUhHddZH0jNdLYtN-3fj-UEJVEIu6dCx1AEM
> .
@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:NP247809.RATVeApVNcUhHddZH0jNdLYtN-3fj-UEJVEIu6dCx1AEM130_head
{
this:
np:hasAssertion
dgn-np:NP247809.RATVeApVNcUhHddZH0jNdLYtN-3fj-UEJVEIu6dCx1AEM130_assertion
;
np:hasProvenance
dgn-np:NP247809.RATVeApVNcUhHddZH0jNdLYtN-3fj-UEJVEIu6dCx1AEM130_provenance
;
np:hasPublicationInfo
dgn-np:NP247809.RATVeApVNcUhHddZH0jNdLYtN-3fj-UEJVEIu6dCx1AEM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP247809.RATVeApVNcUhHddZH0jNdLYtN-3fj-UEJVEIu6dCx1AEM130_assertion
a
np:Assertion
.
dgn-np:NP247809.RATVeApVNcUhHddZH0jNdLYtN-3fj-UEJVEIu6dCx1AEM130_provenance
a
np:Provenance
.
dgn-np:NP247809.RATVeApVNcUhHddZH0jNdLYtN-3fj-UEJVEIu6dCx1AEM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP247809.RATVeApVNcUhHddZH0jNdLYtN-3fj-UEJVEIu6dCx1AEM130_assertion
{
miriam-gene:6261
a
ncit:C16612
.
lld:C0085580
a
ncit:C7057
.
dgn-gda:DGN8f36cd037eafa091937bada196157fea
sio:SIO_000628
miriam-gene:6261
,
lld:C0085580
;
a
sio:SIO_001121
.
}
dgn-np:NP247809.RATVeApVNcUhHddZH0jNdLYtN-3fj-UEJVEIu6dCx1AEM130_provenance
{
dgn-np:NP247809.RATVeApVNcUhHddZH0jNdLYtN-3fj-UEJVEIu6dCx1AEM130_assertion
dcterms:description
"[Genetic variants of alpha adducin (ADD1) taken alone or in interaction with those of beta (ADD2) and gamma (ADD3) subunits have been associated with primary hypertension in humans and in Milan hypertensive (MHS) rats.]. 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:15474463
;
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:NP247809.RATVeApVNcUhHddZH0jNdLYtN-3fj-UEJVEIu6dCx1AEM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:18+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" .
}