@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP400965.RAbSDMzdRGHg9ljrib7OxrjMkW5gHP44WE5ZeqON64jkw
> .
@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:NP400965.RAbSDMzdRGHg9ljrib7OxrjMkW5gHP44WE5ZeqON64jkw130_head
{
this:
np:hasAssertion
dgn-np:NP400965.RAbSDMzdRGHg9ljrib7OxrjMkW5gHP44WE5ZeqON64jkw130_assertion
;
np:hasProvenance
dgn-np:NP400965.RAbSDMzdRGHg9ljrib7OxrjMkW5gHP44WE5ZeqON64jkw130_provenance
;
np:hasPublicationInfo
dgn-np:NP400965.RAbSDMzdRGHg9ljrib7OxrjMkW5gHP44WE5ZeqON64jkw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP400965.RAbSDMzdRGHg9ljrib7OxrjMkW5gHP44WE5ZeqON64jkw130_assertion
a
np:Assertion
.
dgn-np:NP400965.RAbSDMzdRGHg9ljrib7OxrjMkW5gHP44WE5ZeqON64jkw130_provenance
a
np:Provenance
.
dgn-np:NP400965.RAbSDMzdRGHg9ljrib7OxrjMkW5gHP44WE5ZeqON64jkw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP400965.RAbSDMzdRGHg9ljrib7OxrjMkW5gHP44WE5ZeqON64jkw130_assertion
{
miriam-gene:2837
a
ncit:C16612
.
lld:C2316810
a
ncit:C7057
.
dgn-gda:DGNcce13a8991de9cd6b49bafb767d45b52
sio:SIO_000628
miriam-gene:2837
,
lld:C2316810
;
a
sio:SIO_001121
.
}
dgn-np:NP400965.RAbSDMzdRGHg9ljrib7OxrjMkW5gHP44WE5ZeqON64jkw130_provenance
{
dgn-np:NP400965.RAbSDMzdRGHg9ljrib7OxrjMkW5gHP44WE5ZeqON64jkw130_assertion
dcterms:description
"[The 936CC-1451CC genotype in the 3' UTR showed not only susceptibility for ESRD but also higher plasma VEGF levels and mRNA stability, indicating the contribution of VEGF to chronic kidney disease progression, especially in males.]. 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:16421229
;
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:NP400965.RAbSDMzdRGHg9ljrib7OxrjMkW5gHP44WE5ZeqON64jkw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:59+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" .
}