@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1316003.RA8lQnqZzOCBJDkUUQ-fZrDDQO7p6Ax5xc-e35dlBgyHE
> .
@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/
> .
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{
this:
np:hasAssertion
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;
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np:hasPublicationInfo
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a
np:Nanopublication
.
dgn-np:NP1316003.RA8lQnqZzOCBJDkUUQ-fZrDDQO7p6Ax5xc-e35dlBgyHE130_assertion
a
np:Assertion
.
dgn-np:NP1316003.RA8lQnqZzOCBJDkUUQ-fZrDDQO7p6Ax5xc-e35dlBgyHE130_provenance
a
np:Provenance
.
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a
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{
miriam-gene:5972
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN34d5dcfe98d2734187d78f389368bb70
sio:SIO_000628
miriam-gene:5972
,
lld:C0020538
;
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.
}
dgn-np:NP1316003.RA8lQnqZzOCBJDkUUQ-fZrDDQO7p6Ax5xc-e35dlBgyHE130_provenance
{
dgn-np:NP1316003.RA8lQnqZzOCBJDkUUQ-fZrDDQO7p6Ax5xc-e35dlBgyHE130_assertion
dcterms:description
"[We studied the distribution of the SA gene alleles (A1, A2), defined by the PstI polymorphism, in young adults with contrasting predisposition to hypertension to determine whether genetic variation at the SA gene locus is associated with variations in renal haemodynamics, electrolyte metabolism and the renin-angiotensin system.]. 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:7634749
;
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:NP1316003.RA8lQnqZzOCBJDkUUQ-fZrDDQO7p6Ax5xc-e35dlBgyHE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:42+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
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;
pav:authoredBy
<
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> , <
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> , <
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
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"v4.0.0" .
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