@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP758410.RAXOyuaUP0fClmpsL8H0WBamkygczk8h7J5FscJeAUozk
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP758410.RAXOyuaUP0fClmpsL8H0WBamkygczk8h7J5FscJeAUozk130_head
{
this:
np:hasAssertion
dgn-np:NP758410.RAXOyuaUP0fClmpsL8H0WBamkygczk8h7J5FscJeAUozk130_assertion
;
np:hasProvenance
dgn-np:NP758410.RAXOyuaUP0fClmpsL8H0WBamkygczk8h7J5FscJeAUozk130_provenance
;
np:hasPublicationInfo
dgn-np:NP758410.RAXOyuaUP0fClmpsL8H0WBamkygczk8h7J5FscJeAUozk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP758410.RAXOyuaUP0fClmpsL8H0WBamkygczk8h7J5FscJeAUozk130_assertion
a
np:Assertion
.
dgn-np:NP758410.RAXOyuaUP0fClmpsL8H0WBamkygczk8h7J5FscJeAUozk130_provenance
a
np:Provenance
.
dgn-np:NP758410.RAXOyuaUP0fClmpsL8H0WBamkygczk8h7J5FscJeAUozk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP758410.RAXOyuaUP0fClmpsL8H0WBamkygczk8h7J5FscJeAUozk130_assertion
{
miriam-gene:7225
a
ncit:C16612
.
lld:C2919166
a
ncit:C7057
.
dgn-gda:DGNfbc3f1b31f5dc2ec80e6e41e5c4ada0b
sio:SIO_000628
miriam-gene:7225
,
lld:C2919166
;
a
sio:SIO_001121
.
}
dgn-np:NP758410.RAXOyuaUP0fClmpsL8H0WBamkygczk8h7J5FscJeAUozk130_provenance
{
dgn-np:NP758410.RAXOyuaUP0fClmpsL8H0WBamkygczk8h7J5FscJeAUozk130_assertion
dcterms:description
"[Gain-of-function mutations in the calcium channel TRPC6 lead to autosomal dominant focal segmental glomerulosclerosis and podocyte expression of TRPC6 is increased in some acquired human glomerular diseases, particularly in membranous nephropathy.]. 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:24194522
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP758410.RAXOyuaUP0fClmpsL8H0WBamkygczk8h7J5FscJeAUozk130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:17+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}