@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP59230.RA_O08GCz8Ius8mO4jtu_Ng3WGr0mG_rlVmKiKWJV3EoY
> .
@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 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:NP59230.RA_O08GCz8Ius8mO4jtu_Ng3WGr0mG_rlVmKiKWJV3EoY130_head
{
this:
np:hasAssertion
dgn-np:NP59230.RA_O08GCz8Ius8mO4jtu_Ng3WGr0mG_rlVmKiKWJV3EoY130_assertion
;
np:hasProvenance
dgn-np:NP59230.RA_O08GCz8Ius8mO4jtu_Ng3WGr0mG_rlVmKiKWJV3EoY130_provenance
;
np:hasPublicationInfo
dgn-np:NP59230.RA_O08GCz8Ius8mO4jtu_Ng3WGr0mG_rlVmKiKWJV3EoY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP59230.RA_O08GCz8Ius8mO4jtu_Ng3WGr0mG_rlVmKiKWJV3EoY130_assertion
a
np:Assertion
.
dgn-np:NP59230.RA_O08GCz8Ius8mO4jtu_Ng3WGr0mG_rlVmKiKWJV3EoY130_provenance
a
np:Provenance
.
dgn-np:NP59230.RA_O08GCz8Ius8mO4jtu_Ng3WGr0mG_rlVmKiKWJV3EoY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP59230.RA_O08GCz8Ius8mO4jtu_Ng3WGr0mG_rlVmKiKWJV3EoY130_assertion
{
miriam-gene:7428
a
ncit:C16612
.
lld:C0740457
a
ncit:C7057
.
dgn-gda:DGN56966a7b19a15b548add54126edfceb3
sio:SIO_000628
miriam-gene:7428
,
lld:C0740457
;
a
sio:SIO_001122
.
}
dgn-np:NP59230.RA_O08GCz8Ius8mO4jtu_Ng3WGr0mG_rlVmKiKWJV3EoY130_provenance
{
dgn-np:NP59230.RA_O08GCz8Ius8mO4jtu_Ng3WGr0mG_rlVmKiKWJV3EoY130_assertion
dct:description
"[ In this study non-significantly increased risks for history of hypertension and use of antihypertensive medication with RCC were observed. The association with hypertension was stronger in RCC patients with VHL mutations, while there was a positive association of diuretics use and risk of RCC without VHL mutations.]. 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:16208141
;
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:NP59230.RA_O08GCz8Ius8mO4jtu_Ng3WGr0mG_rlVmKiKWJV3EoY130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:28+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}