@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP888606.RAxDG0YAPPnEB1Ljy5s4Jz0CKhuuzT0NQwxGGbD3s47Yo
> .
@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:NP888606.RAxDG0YAPPnEB1Ljy5s4Jz0CKhuuzT0NQwxGGbD3s47Yo130_head
{
this:
np:hasAssertion
dgn-np:NP888606.RAxDG0YAPPnEB1Ljy5s4Jz0CKhuuzT0NQwxGGbD3s47Yo130_assertion
;
np:hasProvenance
dgn-np:NP888606.RAxDG0YAPPnEB1Ljy5s4Jz0CKhuuzT0NQwxGGbD3s47Yo130_provenance
;
np:hasPublicationInfo
dgn-np:NP888606.RAxDG0YAPPnEB1Ljy5s4Jz0CKhuuzT0NQwxGGbD3s47Yo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP888606.RAxDG0YAPPnEB1Ljy5s4Jz0CKhuuzT0NQwxGGbD3s47Yo130_assertion
a
np:Assertion
.
dgn-np:NP888606.RAxDG0YAPPnEB1Ljy5s4Jz0CKhuuzT0NQwxGGbD3s47Yo130_provenance
a
np:Provenance
.
dgn-np:NP888606.RAxDG0YAPPnEB1Ljy5s4Jz0CKhuuzT0NQwxGGbD3s47Yo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP888606.RAxDG0YAPPnEB1Ljy5s4Jz0CKhuuzT0NQwxGGbD3s47Yo130_assertion
{
miriam-gene:5972
a
ncit:C16612
.
lld:C0149721
a
ncit:C7057
.
dgn-gda:DGN84cbeecbca622c6146e3d826dccd27d1
sio:SIO_000628
miriam-gene:5972
,
lld:C0149721
;
a
sio:SIO_001121
.
}
dgn-np:NP888606.RAxDG0YAPPnEB1Ljy5s4Jz0CKhuuzT0NQwxGGbD3s47Yo130_provenance
{
dgn-np:NP888606.RAxDG0YAPPnEB1Ljy5s4Jz0CKhuuzT0NQwxGGbD3s47Yo130_assertion
dcterms:description
"[Polymorphisms of the renin-angiotensin-aldosterone system (RAAS) represent an attractive hypothesis as potential disease modifiers, as these genetic variants alter the 'activation status' of the RAAS, which leads to more left ventricular hypertrophy through different pathways.]. 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:21507890
;
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:NP888606.RAxDG0YAPPnEB1Ljy5s4Jz0CKhuuzT0NQwxGGbD3s47Yo130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:27+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" .
}