@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP535742.RABoZY4nhdOJ0bLYzCcultD1nWMX5eHf-8m-pJFITuPIE
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP535742.RABoZY4nhdOJ0bLYzCcultD1nWMX5eHf-8m-pJFITuPIE130_assertion
;
np:hasProvenance
dgn-np:NP535742.RABoZY4nhdOJ0bLYzCcultD1nWMX5eHf-8m-pJFITuPIE130_provenance
;
np:hasPublicationInfo
dgn-np:NP535742.RABoZY4nhdOJ0bLYzCcultD1nWMX5eHf-8m-pJFITuPIE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP535742.RABoZY4nhdOJ0bLYzCcultD1nWMX5eHf-8m-pJFITuPIE130_assertion
a
np:Assertion
.
dgn-np:NP535742.RABoZY4nhdOJ0bLYzCcultD1nWMX5eHf-8m-pJFITuPIE130_provenance
a
np:Provenance
.
dgn-np:NP535742.RABoZY4nhdOJ0bLYzCcultD1nWMX5eHf-8m-pJFITuPIE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP535742.RABoZY4nhdOJ0bLYzCcultD1nWMX5eHf-8m-pJFITuPIE130_assertion
{
miriam-gene:7124
a
ncit:C16612
.
lld:C0011881
a
ncit:C7057
.
dgn-gda:DGNa32f9f9571d147715eae297f1504905f
sio:SIO_000628
miriam-gene:7124
,
lld:C0011881
;
a
sio:SIO_001121
.
}
dgn-np:NP535742.RABoZY4nhdOJ0bLYzCcultD1nWMX5eHf-8m-pJFITuPIE130_provenance
{
dgn-np:NP535742.RABoZY4nhdOJ0bLYzCcultD1nWMX5eHf-8m-pJFITuPIE130_assertion
dcterms:description
"[In conclusion, we found that in diabetic nephropathy patients molecular variants of TNF are more frequent than in nondiabetic patients with chronic renal failure and these changes might be associated with altered ability to TNF synthesis.]. 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:15600254
;
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:NP535742.RABoZY4nhdOJ0bLYzCcultD1nWMX5eHf-8m-pJFITuPIE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:23+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" .
}