@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP837638.RAJprUp8DZ-pw3yUSJmypd1EQv0hW1MXJ3j5DM3n1xjYE
> .
@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:NP837638.RAJprUp8DZ-pw3yUSJmypd1EQv0hW1MXJ3j5DM3n1xjYE130_head
{
this:
np:hasAssertion
dgn-np:NP837638.RAJprUp8DZ-pw3yUSJmypd1EQv0hW1MXJ3j5DM3n1xjYE130_assertion
;
np:hasProvenance
dgn-np:NP837638.RAJprUp8DZ-pw3yUSJmypd1EQv0hW1MXJ3j5DM3n1xjYE130_provenance
;
np:hasPublicationInfo
dgn-np:NP837638.RAJprUp8DZ-pw3yUSJmypd1EQv0hW1MXJ3j5DM3n1xjYE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP837638.RAJprUp8DZ-pw3yUSJmypd1EQv0hW1MXJ3j5DM3n1xjYE130_assertion
a
np:Assertion
.
dgn-np:NP837638.RAJprUp8DZ-pw3yUSJmypd1EQv0hW1MXJ3j5DM3n1xjYE130_provenance
a
np:Provenance
.
dgn-np:NP837638.RAJprUp8DZ-pw3yUSJmypd1EQv0hW1MXJ3j5DM3n1xjYE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP837638.RAJprUp8DZ-pw3yUSJmypd1EQv0hW1MXJ3j5DM3n1xjYE130_assertion
{
miriam-gene:81
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGNa169878f4bfffec5181807fd3259e395
sio:SIO_000628
miriam-gene:81
,
lld:C0020538
;
a
sio:SIO_001121
.
}
dgn-np:NP837638.RAJprUp8DZ-pw3yUSJmypd1EQv0hW1MXJ3j5DM3n1xjYE130_provenance
{
dgn-np:NP837638.RAJprUp8DZ-pw3yUSJmypd1EQv0hW1MXJ3j5DM3n1xjYE130_assertion
dcterms:description
"[Statistically stronger associations were detected between two independent sequence variants in the Apolipoprotein L1 gene (APOL1) and nondiabetic nephropathy in African Americans, with odds ratios of 10.5 in idiopathic FSGS and 7.3 in hypertension-attributed ESRD.]. 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:20688934
;
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:NP837638.RAJprUp8DZ-pw3yUSJmypd1EQv0hW1MXJ3j5DM3n1xjYE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:32+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" .
}