@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP916545.RAnHwadt4F8NGzNa9UuUeel2LXa6lat6XeCMhk0NR0Mio
> .
@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:NP916545.RAnHwadt4F8NGzNa9UuUeel2LXa6lat6XeCMhk0NR0Mio130_head
{
this:
np:hasAssertion
dgn-np:NP916545.RAnHwadt4F8NGzNa9UuUeel2LXa6lat6XeCMhk0NR0Mio130_assertion
;
np:hasProvenance
dgn-np:NP916545.RAnHwadt4F8NGzNa9UuUeel2LXa6lat6XeCMhk0NR0Mio130_provenance
;
np:hasPublicationInfo
dgn-np:NP916545.RAnHwadt4F8NGzNa9UuUeel2LXa6lat6XeCMhk0NR0Mio130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP916545.RAnHwadt4F8NGzNa9UuUeel2LXa6lat6XeCMhk0NR0Mio130_assertion
a
np:Assertion
.
dgn-np:NP916545.RAnHwadt4F8NGzNa9UuUeel2LXa6lat6XeCMhk0NR0Mio130_provenance
a
np:Provenance
.
dgn-np:NP916545.RAnHwadt4F8NGzNa9UuUeel2LXa6lat6XeCMhk0NR0Mio130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP916545.RAnHwadt4F8NGzNa9UuUeel2LXa6lat6XeCMhk0NR0Mio130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0035078
a
ncit:C7057
.
dgn-gda:DGN741b41efdc30aec548989fbb77beb308
sio:SIO_000628
miriam-gene:348
,
lld:C0035078
;
a
sio:SIO_001121
.
}
dgn-np:NP916545.RAnHwadt4F8NGzNa9UuUeel2LXa6lat6XeCMhk0NR0Mio130_provenance
{
dgn-np:NP916545.RAnHwadt4F8NGzNa9UuUeel2LXa6lat6XeCMhk0NR0Mio130_assertion
dcterms:description
"[Lipoprotein glomerulopathy is clinically characterized by proteinuria and progression to renal failure and is caused by glomerular lipoprotein thrombi formation in association with increased levels of serum apolipoprotein E. The disease has a male predominance and can affect virtually any age group.]. 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:20121619
;
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:NP916545.RAnHwadt4F8NGzNa9UuUeel2LXa6lat6XeCMhk0NR0Mio130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:22+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" .
}