@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP91028.RACWk__Oss_o51Vbbq215nvxSc77GCsNfy_XUi4tj4gac
> .
@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:NP91028.RACWk__Oss_o51Vbbq215nvxSc77GCsNfy_XUi4tj4gac130_head
{
this:
np:hasAssertion
dgn-np:NP91028.RACWk__Oss_o51Vbbq215nvxSc77GCsNfy_XUi4tj4gac130_assertion
;
np:hasProvenance
dgn-np:NP91028.RACWk__Oss_o51Vbbq215nvxSc77GCsNfy_XUi4tj4gac130_provenance
;
np:hasPublicationInfo
dgn-np:NP91028.RACWk__Oss_o51Vbbq215nvxSc77GCsNfy_XUi4tj4gac130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP91028.RACWk__Oss_o51Vbbq215nvxSc77GCsNfy_XUi4tj4gac130_assertion
a
np:Assertion
.
dgn-np:NP91028.RACWk__Oss_o51Vbbq215nvxSc77GCsNfy_XUi4tj4gac130_provenance
a
np:Provenance
.
dgn-np:NP91028.RACWk__Oss_o51Vbbq215nvxSc77GCsNfy_XUi4tj4gac130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP91028.RACWk__Oss_o51Vbbq215nvxSc77GCsNfy_XUi4tj4gac130_assertion
{
miriam-gene:80833
a
ncit:C16612
.
lld:C0376358
a
ncit:C7057
.
dgn-gda:DGNf6a3dc15bf49c6757e3a004fb454d340
sio:SIO_000628
miriam-gene:80833
,
lld:C0376358
;
a
sio:SIO_001122
.
}
dgn-np:NP91028.RACWk__Oss_o51Vbbq215nvxSc77GCsNfy_XUi4tj4gac130_provenance
{
dgn-np:NP91028.RACWk__Oss_o51Vbbq215nvxSc77GCsNfy_XUi4tj4gac130_assertion
dcterms:description
"[The two independent sets of HPC cases highlight the same 15 kb interval at the 5' end of the APOL3 gene and provide strong evidence that SNPs within this 15 kb interval, or in strong linkage disequilibrium with it, contribute to HPC risk.]. 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:20631155
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP91028.RACWk__Oss_o51Vbbq215nvxSc77GCsNfy_XUi4tj4gac130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:45+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" .
}