@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP662194.RA8JHSoiNO3FSJbEaJrwlfx6Q49eMqo96u9TtbiMwu9rs
> .
@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:NP662194.RA8JHSoiNO3FSJbEaJrwlfx6Q49eMqo96u9TtbiMwu9rs130_head
{
this:
np:hasAssertion
dgn-np:NP662194.RA8JHSoiNO3FSJbEaJrwlfx6Q49eMqo96u9TtbiMwu9rs130_assertion
;
np:hasProvenance
dgn-np:NP662194.RA8JHSoiNO3FSJbEaJrwlfx6Q49eMqo96u9TtbiMwu9rs130_provenance
;
np:hasPublicationInfo
dgn-np:NP662194.RA8JHSoiNO3FSJbEaJrwlfx6Q49eMqo96u9TtbiMwu9rs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP662194.RA8JHSoiNO3FSJbEaJrwlfx6Q49eMqo96u9TtbiMwu9rs130_assertion
a
np:Assertion
.
dgn-np:NP662194.RA8JHSoiNO3FSJbEaJrwlfx6Q49eMqo96u9TtbiMwu9rs130_provenance
a
np:Provenance
.
dgn-np:NP662194.RA8JHSoiNO3FSJbEaJrwlfx6Q49eMqo96u9TtbiMwu9rs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP662194.RA8JHSoiNO3FSJbEaJrwlfx6Q49eMqo96u9TtbiMwu9rs130_assertion
{
miriam-gene:23771
a
ncit:C16612
.
lld:C0152451
a
ncit:C7057
.
dgn-gda:DGN422596a466eef5a3a9ae53b82fbce368
sio:SIO_000628
miriam-gene:23771
,
lld:C0152451
;
a
sio:SIO_001121
.
}
dgn-np:NP662194.RA8JHSoiNO3FSJbEaJrwlfx6Q49eMqo96u9TtbiMwu9rs130_provenance
{
dgn-np:NP662194.RA8JHSoiNO3FSJbEaJrwlfx6Q49eMqo96u9TtbiMwu9rs130_assertion
dcterms:description
"[Genotyping the -463G/A polymorphism in HN, chronic glomerulonephritis (CGN) and diabetic nephropathy (DM) patients who were under hemodialysis treatment demonstrated that the GG genotype was more frequent in the HN group than in the CGN and DM groups.]. 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:18344624
;
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:NP662194.RA8JHSoiNO3FSJbEaJrwlfx6Q49eMqo96u9TtbiMwu9rs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:40+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" .
}