@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1385630.RAD5T1Ln249xz44SmpCggWpUtBfwFBGinHR84YP16dDNA
> .
@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:NP1385630.RAD5T1Ln249xz44SmpCggWpUtBfwFBGinHR84YP16dDNA130_head
{
this:
np:hasAssertion
dgn-np:NP1385630.RAD5T1Ln249xz44SmpCggWpUtBfwFBGinHR84YP16dDNA130_assertion
;
np:hasProvenance
dgn-np:NP1385630.RAD5T1Ln249xz44SmpCggWpUtBfwFBGinHR84YP16dDNA130_provenance
;
np:hasPublicationInfo
dgn-np:NP1385630.RAD5T1Ln249xz44SmpCggWpUtBfwFBGinHR84YP16dDNA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1385630.RAD5T1Ln249xz44SmpCggWpUtBfwFBGinHR84YP16dDNA130_assertion
a
np:Assertion
.
dgn-np:NP1385630.RAD5T1Ln249xz44SmpCggWpUtBfwFBGinHR84YP16dDNA130_provenance
a
np:Provenance
.
dgn-np:NP1385630.RAD5T1Ln249xz44SmpCggWpUtBfwFBGinHR84YP16dDNA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1385630.RAD5T1Ln249xz44SmpCggWpUtBfwFBGinHR84YP16dDNA130_assertion
{
miriam-gene:189
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGNe3fda91a5bdbd85039b25a15e6830fff
sio:SIO_000628
miriam-gene:189
,
lld:C0020538
;
a
sio:SIO_001121
.
}
dgn-np:NP1385630.RAD5T1Ln249xz44SmpCggWpUtBfwFBGinHR84YP16dDNA130_provenance
{
dgn-np:NP1385630.RAD5T1Ln249xz44SmpCggWpUtBfwFBGinHR84YP16dDNA130_assertion
dcterms:description
"[Despite a statistically significant, albeit weak, association between the AGT 235T variant and hypertension that has been confirmed through sensitivity analysis, this finding has to be interpreted with caution, as the methodological weaknesses of the individual studies are likely to have biased the outcome of the meta-analysis.]. 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:9403549
;
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:NP1385630.RAD5T1Ln249xz44SmpCggWpUtBfwFBGinHR84YP16dDNA130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:14+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" .
}