@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP434008.RAAGzqFOGVaEPDrI9pvAeGGNPhYTpsWfEKy7oRKDkVpbI
> .
@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:NP434008.RAAGzqFOGVaEPDrI9pvAeGGNPhYTpsWfEKy7oRKDkVpbI130_head
{
this:
np:hasAssertion
dgn-np:NP434008.RAAGzqFOGVaEPDrI9pvAeGGNPhYTpsWfEKy7oRKDkVpbI130_assertion
;
np:hasProvenance
dgn-np:NP434008.RAAGzqFOGVaEPDrI9pvAeGGNPhYTpsWfEKy7oRKDkVpbI130_provenance
;
np:hasPublicationInfo
dgn-np:NP434008.RAAGzqFOGVaEPDrI9pvAeGGNPhYTpsWfEKy7oRKDkVpbI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP434008.RAAGzqFOGVaEPDrI9pvAeGGNPhYTpsWfEKy7oRKDkVpbI130_assertion
a
np:Assertion
.
dgn-np:NP434008.RAAGzqFOGVaEPDrI9pvAeGGNPhYTpsWfEKy7oRKDkVpbI130_provenance
a
np:Provenance
.
dgn-np:NP434008.RAAGzqFOGVaEPDrI9pvAeGGNPhYTpsWfEKy7oRKDkVpbI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP434008.RAAGzqFOGVaEPDrI9pvAeGGNPhYTpsWfEKy7oRKDkVpbI130_assertion
{
miriam-gene:11093
a
ncit:C16612
.
lld:C0398623
a
ncit:C7057
.
dgn-gda:DGN6d681d24a874bbe3908a18533e35016e
sio:SIO_000628
miriam-gene:11093
,
lld:C0398623
;
a
sio:SIO_001121
.
}
dgn-np:NP434008.RAAGzqFOGVaEPDrI9pvAeGGNPhYTpsWfEKy7oRKDkVpbI130_provenance
{
dgn-np:NP434008.RAAGzqFOGVaEPDrI9pvAeGGNPhYTpsWfEKy7oRKDkVpbI130_assertion
dcterms:description
"[Recent studies have shown that increased plasma levels of Von Willebrand factor (VWF) and reduced plasma levels of enzyme ADAMTS13 are associated with diabetic nephropathy and an increased risk of developing cardiovascular disease, suggesting that these markers of hypercoagulability may contribute to an increased risk of cardiovascular disease in diabetic patients with impaired renal function.]. 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:23159842
;
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:NP434008.RAAGzqFOGVaEPDrI9pvAeGGNPhYTpsWfEKy7oRKDkVpbI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:17+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" .
}