@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP55795.RAHcj25kWS5awAl4Ka95aACw0Mavm_8hSC6WdirZZ5GPw
> .
@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/v3.0.0/void/
> .
dgn-np:NP55795.RAHcj25kWS5awAl4Ka95aACw0Mavm_8hSC6WdirZZ5GPw130_head
{
this:
np:hasAssertion
dgn-np:NP55795.RAHcj25kWS5awAl4Ka95aACw0Mavm_8hSC6WdirZZ5GPw130_assertion
;
np:hasProvenance
dgn-np:NP55795.RAHcj25kWS5awAl4Ka95aACw0Mavm_8hSC6WdirZZ5GPw130_provenance
;
np:hasPublicationInfo
dgn-np:NP55795.RAHcj25kWS5awAl4Ka95aACw0Mavm_8hSC6WdirZZ5GPw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP55795.RAHcj25kWS5awAl4Ka95aACw0Mavm_8hSC6WdirZZ5GPw130_assertion
a
np:Assertion
.
dgn-np:NP55795.RAHcj25kWS5awAl4Ka95aACw0Mavm_8hSC6WdirZZ5GPw130_provenance
a
np:Provenance
.
dgn-np:NP55795.RAHcj25kWS5awAl4Ka95aACw0Mavm_8hSC6WdirZZ5GPw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP55795.RAHcj25kWS5awAl4Ka95aACw0Mavm_8hSC6WdirZZ5GPw130_assertion
{
miriam-gene:1535
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGNea3d978f0e6738fd504aa98fb7b762fe
sio:SIO_000628
miriam-gene:1535
,
lld:C0020538
;
a
sio:SIO_001122
.
}
dgn-np:NP55795.RAHcj25kWS5awAl4Ka95aACw0Mavm_8hSC6WdirZZ5GPw130_provenance
{
dgn-np:NP55795.RAHcj25kWS5awAl4Ka95aACw0Mavm_8hSC6WdirZZ5GPw130_assertion
dcterms:description
"[The aim of the study was to analyze the prevalence of polymorphism Glu298Asp of endothelial nitric oxide synthase gene and C242T p22 phox polymorphism of NADPH oxidase gene in patients with arterial hypertension (AH) and their influence on AH complications.]. 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:18429753
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP55795.RAHcj25kWS5awAl4Ka95aACw0Mavm_8hSC6WdirZZ5GPw130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:10+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}