@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1152498.RAFeiUt_gcPeCfjW1AX8cR3eIlfQg3qmoJlIgByjYSGZ0
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1152498.RAFeiUt_gcPeCfjW1AX8cR3eIlfQg3qmoJlIgByjYSGZ0130_head
{
this:
np:hasAssertion
dgn-np:NP1152498.RAFeiUt_gcPeCfjW1AX8cR3eIlfQg3qmoJlIgByjYSGZ0130_assertion
;
np:hasProvenance
dgn-np:NP1152498.RAFeiUt_gcPeCfjW1AX8cR3eIlfQg3qmoJlIgByjYSGZ0130_provenance
;
np:hasPublicationInfo
dgn-np:NP1152498.RAFeiUt_gcPeCfjW1AX8cR3eIlfQg3qmoJlIgByjYSGZ0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1152498.RAFeiUt_gcPeCfjW1AX8cR3eIlfQg3qmoJlIgByjYSGZ0130_assertion
a
np:Assertion
.
dgn-np:NP1152498.RAFeiUt_gcPeCfjW1AX8cR3eIlfQg3qmoJlIgByjYSGZ0130_provenance
a
np:Provenance
.
dgn-np:NP1152498.RAFeiUt_gcPeCfjW1AX8cR3eIlfQg3qmoJlIgByjYSGZ0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1152498.RAFeiUt_gcPeCfjW1AX8cR3eIlfQg3qmoJlIgByjYSGZ0130_assertion
{
miriam-gene:8542
a
ncit:C16612
.
lld:C0017668
a
ncit:C7057
.
dgn-gda:DGN63af7e6f28de9fafb701c5354e6851e1
sio:SIO_000628
miriam-gene:8542
,
lld:C0017668
;
a
sio:SIO_001121
.
}
dgn-np:NP1152498.RAFeiUt_gcPeCfjW1AX8cR3eIlfQg3qmoJlIgByjYSGZ0130_provenance
{
dgn-np:NP1152498.RAFeiUt_gcPeCfjW1AX8cR3eIlfQg3qmoJlIgByjYSGZ0130_assertion
dcterms:description
"[The prevalence of pathogenic mutations in five genes (NPHS2, TRPC6, ACTN4, INF2 and PLCE1) and of APOL1 risk alleles (G1 and G2) was ascertained in children and adults diagnosed between 1984 and 2011 with FSGS by renal biopsy.]. 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:24500309
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1152498.RAFeiUt_gcPeCfjW1AX8cR3eIlfQg3qmoJlIgByjYSGZ0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:28+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}