@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP424422.RAjPnyyJKjoXIA68F4qVd_NjRZrMlrvRCmdJByusop4Sk
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP424422.RAjPnyyJKjoXIA68F4qVd_NjRZrMlrvRCmdJByusop4Sk130_assertion
;
np:hasProvenance
dgn-np:NP424422.RAjPnyyJKjoXIA68F4qVd_NjRZrMlrvRCmdJByusop4Sk130_provenance
;
np:hasPublicationInfo
dgn-np:NP424422.RAjPnyyJKjoXIA68F4qVd_NjRZrMlrvRCmdJByusop4Sk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP424422.RAjPnyyJKjoXIA68F4qVd_NjRZrMlrvRCmdJByusop4Sk130_assertion
a
np:Assertion
.
dgn-np:NP424422.RAjPnyyJKjoXIA68F4qVd_NjRZrMlrvRCmdJByusop4Sk130_provenance
a
np:Provenance
.
dgn-np:NP424422.RAjPnyyJKjoXIA68F4qVd_NjRZrMlrvRCmdJByusop4Sk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP424422.RAjPnyyJKjoXIA68F4qVd_NjRZrMlrvRCmdJByusop4Sk130_assertion
{
miriam-gene:4627
a
ncit:C16612
.
lld:C2316810
a
ncit:C7057
.
dgn-gda:DGN8686c315d92e1b90d5285ec9282dea81
sio:SIO_000628
miriam-gene:4627
,
lld:C2316810
;
a
sio:SIO_001121
.
}
dgn-np:NP424422.RAjPnyyJKjoXIA68F4qVd_NjRZrMlrvRCmdJByusop4Sk130_provenance
{
dgn-np:NP424422.RAjPnyyJKjoXIA68F4qVd_NjRZrMlrvRCmdJByusop4Sk130_assertion
dcterms:description
"[This led us to re-examine the interval surrounding MYH9 and to the detection of novel missense mutations with predicted functional effects in the neighboring APOL1 gene, which are significantly more associated with ESKD than all previously reported SNPs in MYH9.]. 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:20635188
;
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:NP424422.RAjPnyyJKjoXIA68F4qVd_NjRZrMlrvRCmdJByusop4Sk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:12+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
<
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> , <
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
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"v2.1.0" .
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