@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP411344.RAq3cN-fmSRtKCAzm_jHbFOcORyObjnkTFpUiYpDJ08NI
> .
@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:NP411344.RAq3cN-fmSRtKCAzm_jHbFOcORyObjnkTFpUiYpDJ08NI130_head
{
this:
np:hasAssertion
dgn-np:NP411344.RAq3cN-fmSRtKCAzm_jHbFOcORyObjnkTFpUiYpDJ08NI130_assertion
;
np:hasProvenance
dgn-np:NP411344.RAq3cN-fmSRtKCAzm_jHbFOcORyObjnkTFpUiYpDJ08NI130_provenance
;
np:hasPublicationInfo
dgn-np:NP411344.RAq3cN-fmSRtKCAzm_jHbFOcORyObjnkTFpUiYpDJ08NI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP411344.RAq3cN-fmSRtKCAzm_jHbFOcORyObjnkTFpUiYpDJ08NI130_assertion
a
np:Assertion
.
dgn-np:NP411344.RAq3cN-fmSRtKCAzm_jHbFOcORyObjnkTFpUiYpDJ08NI130_provenance
a
np:Provenance
.
dgn-np:NP411344.RAq3cN-fmSRtKCAzm_jHbFOcORyObjnkTFpUiYpDJ08NI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP411344.RAq3cN-fmSRtKCAzm_jHbFOcORyObjnkTFpUiYpDJ08NI130_assertion
{
miriam-gene:574045
a
ncit:C16612
.
lld:C0011849
a
ncit:C7057
.
dgn-gda:DGN6a02434d72fde9ddb14bf583da746ecd
sio:SIO_000628
miriam-gene:574045
,
lld:C0011849
;
a
sio:SIO_001121
.
}
dgn-np:NP411344.RAq3cN-fmSRtKCAzm_jHbFOcORyObjnkTFpUiYpDJ08NI130_provenance
{
dgn-np:NP411344.RAq3cN-fmSRtKCAzm_jHbFOcORyObjnkTFpUiYpDJ08NI130_assertion
dcterms:description
"[A total of 155 Hispanic living kidney donors as controls and a total of 86 Hispanic kidney transplant patients, whose renal failure was attributed to hypertensive nephropathy after ruling out diabetes mellitus or other causes, were genotyped for four different single nucleotide polymorphisms of VEGF: -2578 C>A (rs699947), -1154 G>A (rs1570360), -460 C>T (rs833061), and +936 C>T (rs3025039).]. 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:21080079
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP411344.RAq3cN-fmSRtKCAzm_jHbFOcORyObjnkTFpUiYpDJ08NI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:04+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" .
}