@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP509924.RAbhQeJvjZaeAU40T6affrqKC-eAYNtCaxWRbfE2ATbfE
> .
@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:NP509924.RAbhQeJvjZaeAU40T6affrqKC-eAYNtCaxWRbfE2ATbfE130_head
{
this:
np:hasAssertion
dgn-np:NP509924.RAbhQeJvjZaeAU40T6affrqKC-eAYNtCaxWRbfE2ATbfE130_assertion
;
np:hasProvenance
dgn-np:NP509924.RAbhQeJvjZaeAU40T6affrqKC-eAYNtCaxWRbfE2ATbfE130_provenance
;
np:hasPublicationInfo
dgn-np:NP509924.RAbhQeJvjZaeAU40T6affrqKC-eAYNtCaxWRbfE2ATbfE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP509924.RAbhQeJvjZaeAU40T6affrqKC-eAYNtCaxWRbfE2ATbfE130_assertion
a
np:Assertion
.
dgn-np:NP509924.RAbhQeJvjZaeAU40T6affrqKC-eAYNtCaxWRbfE2ATbfE130_provenance
a
np:Provenance
.
dgn-np:NP509924.RAbhQeJvjZaeAU40T6affrqKC-eAYNtCaxWRbfE2ATbfE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP509924.RAbhQeJvjZaeAU40T6affrqKC-eAYNtCaxWRbfE2ATbfE130_assertion
{
miriam-gene:7827
a
ncit:C16612
.
lld:C1458156
a
ncit:C7057
.
dgn-gda:DGNa35082d627b0d52c4b128d23576843dc
sio:SIO_000628
miriam-gene:7827
,
lld:C1458156
;
a
sio:SIO_001121
.
}
dgn-np:NP509924.RAbhQeJvjZaeAU40T6affrqKC-eAYNtCaxWRbfE2ATbfE130_provenance
{
dgn-np:NP509924.RAbhQeJvjZaeAU40T6affrqKC-eAYNtCaxWRbfE2ATbfE130_assertion
dcterms:description
"[This observation confirms the concept that recurrence of proteinuria may occur in inherited forms of FSGS so far reported only for patients carrying NPHS2 mutations and reinforces the idea on multifactorial origin of the disease.]. 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:16780544
;
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:NP509924.RAbhQeJvjZaeAU40T6affrqKC-eAYNtCaxWRbfE2ATbfE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:04+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" .
}