@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP53312.RAVvWuzzseWjZq2KyO9qO1UFMeyADoYmZaLIx_hSdUkvE
> .
@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:NP53312.RAVvWuzzseWjZq2KyO9qO1UFMeyADoYmZaLIx_hSdUkvE130_head
{
this:
np:hasAssertion
dgn-np:NP53312.RAVvWuzzseWjZq2KyO9qO1UFMeyADoYmZaLIx_hSdUkvE130_assertion
;
np:hasProvenance
dgn-np:NP53312.RAVvWuzzseWjZq2KyO9qO1UFMeyADoYmZaLIx_hSdUkvE130_provenance
;
np:hasPublicationInfo
dgn-np:NP53312.RAVvWuzzseWjZq2KyO9qO1UFMeyADoYmZaLIx_hSdUkvE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP53312.RAVvWuzzseWjZq2KyO9qO1UFMeyADoYmZaLIx_hSdUkvE130_assertion
a
np:Assertion
.
dgn-np:NP53312.RAVvWuzzseWjZq2KyO9qO1UFMeyADoYmZaLIx_hSdUkvE130_provenance
a
np:Provenance
.
dgn-np:NP53312.RAVvWuzzseWjZq2KyO9qO1UFMeyADoYmZaLIx_hSdUkvE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP53312.RAVvWuzzseWjZq2KyO9qO1UFMeyADoYmZaLIx_hSdUkvE130_assertion
{
miriam-gene:5126
a
ncit:C16612
.
lld:C0011860
a
ncit:C7057
.
dgn-gda:DGNeff8d94028f1083616a8c0c1122ff29b
sio:SIO_000628
miriam-gene:5126
,
lld:C0011860
;
a
sio:SIO_001122
.
}
dgn-np:NP53312.RAVvWuzzseWjZq2KyO9qO1UFMeyADoYmZaLIx_hSdUkvE130_provenance
{
dgn-np:NP53312.RAVvWuzzseWjZq2KyO9qO1UFMeyADoYmZaLIx_hSdUkvE130_assertion
dcterms:description
"[Genetic variation may modify the risk of death on dialysis. SNPs in proximity to genes regulating vascular extracellular matrix, cardiac ventricular repolarization, and smoking cessation are associated with dialysis survival in AAs with T2D. These results warrant replication in other cohorts and races.]. 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:21546767
;
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:NP53312.RAVvWuzzseWjZq2KyO9qO1UFMeyADoYmZaLIx_hSdUkvE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:24+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" .
}