@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP49483.RADHXMyQAi7h8v9R8Zx1yl58aWzUM5KmibbGvZ-WTGziA
> .
@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:NP49483.RADHXMyQAi7h8v9R8Zx1yl58aWzUM5KmibbGvZ-WTGziA130_head
{
this:
np:hasAssertion
dgn-np:NP49483.RADHXMyQAi7h8v9R8Zx1yl58aWzUM5KmibbGvZ-WTGziA130_assertion
;
np:hasProvenance
dgn-np:NP49483.RADHXMyQAi7h8v9R8Zx1yl58aWzUM5KmibbGvZ-WTGziA130_provenance
;
np:hasPublicationInfo
dgn-np:NP49483.RADHXMyQAi7h8v9R8Zx1yl58aWzUM5KmibbGvZ-WTGziA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP49483.RADHXMyQAi7h8v9R8Zx1yl58aWzUM5KmibbGvZ-WTGziA130_assertion
a
np:Assertion
.
dgn-np:NP49483.RADHXMyQAi7h8v9R8Zx1yl58aWzUM5KmibbGvZ-WTGziA130_provenance
a
np:Provenance
.
dgn-np:NP49483.RADHXMyQAi7h8v9R8Zx1yl58aWzUM5KmibbGvZ-WTGziA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP49483.RADHXMyQAi7h8v9R8Zx1yl58aWzUM5KmibbGvZ-WTGziA130_assertion
{
miriam-gene:1636
a
ncit:C16612
.
lld:C0022658
a
ncit:C7057
.
dgn-gda:DGN0dbb49063c80ade7ca1ea5aa6dcf8439
sio:SIO_000628
miriam-gene:1636
,
lld:C0022658
;
a
sio:SIO_001122
.
}
dgn-np:NP49483.RADHXMyQAi7h8v9R8Zx1yl58aWzUM5KmibbGvZ-WTGziA130_provenance
{
dgn-np:NP49483.RADHXMyQAi7h8v9R8Zx1yl58aWzUM5KmibbGvZ-WTGziA130_assertion
dcterms:description
"[In our studies on the hypertension in kidney disease we have choosen the evaluation of incidence of hypertension in the early stage of primary glomerulonephritis (GN) and the comparison of distribution of genotypes and alleles depending on insertion/deletion polymorphism of angiotensin converting enzyme (ACE) gene in patients with early stage of GN and healthy subjects.]. 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:14974362
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP49483.RADHXMyQAi7h8v9R8Zx1yl58aWzUM5KmibbGvZ-WTGziA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:22+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" .
}