@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP564383.RAwmbgq21Q-EI0v9VEzXM9OBJLQU3XkUMyM7evZmkCZDw
> .
@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:NP564383.RAwmbgq21Q-EI0v9VEzXM9OBJLQU3XkUMyM7evZmkCZDw130_head
{
this:
np:hasAssertion
dgn-np:NP564383.RAwmbgq21Q-EI0v9VEzXM9OBJLQU3XkUMyM7evZmkCZDw130_assertion
;
np:hasProvenance
dgn-np:NP564383.RAwmbgq21Q-EI0v9VEzXM9OBJLQU3XkUMyM7evZmkCZDw130_provenance
;
np:hasPublicationInfo
dgn-np:NP564383.RAwmbgq21Q-EI0v9VEzXM9OBJLQU3XkUMyM7evZmkCZDw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP564383.RAwmbgq21Q-EI0v9VEzXM9OBJLQU3XkUMyM7evZmkCZDw130_assertion
a
np:Assertion
.
dgn-np:NP564383.RAwmbgq21Q-EI0v9VEzXM9OBJLQU3XkUMyM7evZmkCZDw130_provenance
a
np:Provenance
.
dgn-np:NP564383.RAwmbgq21Q-EI0v9VEzXM9OBJLQU3XkUMyM7evZmkCZDw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP564383.RAwmbgq21Q-EI0v9VEzXM9OBJLQU3XkUMyM7evZmkCZDw130_assertion
{
miriam-gene:5444
a
ncit:C16612
.
lld:C0017668
a
ncit:C7057
.
dgn-gda:DGNce4379a3dadb4e1a6843715384b9cf47
sio:SIO_000628
miriam-gene:5444
,
lld:C0017668
;
a
sio:SIO_001121
.
}
dgn-np:NP564383.RAwmbgq21Q-EI0v9VEzXM9OBJLQU3XkUMyM7evZmkCZDw130_provenance
{
dgn-np:NP564383.RAwmbgq21Q-EI0v9VEzXM9OBJLQU3XkUMyM7evZmkCZDw130_assertion
dcterms:description
"[The aim of this study was to determine the frequency of these genetic polymorphisms in PON1 in Arab and Jewish children with FSGS and to determine any association with severity of outcome.]. 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:11096050
;
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:NP564383.RAwmbgq21Q-EI0v9VEzXM9OBJLQU3XkUMyM7evZmkCZDw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:40+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" .
}