@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP300981.RA9vJ6wS9KTGrFYbiPABlwNTcl8-w3MuvEPUrzz1Rbr90
> .
@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:NP300981.RA9vJ6wS9KTGrFYbiPABlwNTcl8-w3MuvEPUrzz1Rbr90130_head
{
this:
np:hasAssertion
dgn-np:NP300981.RA9vJ6wS9KTGrFYbiPABlwNTcl8-w3MuvEPUrzz1Rbr90130_assertion
;
np:hasProvenance
dgn-np:NP300981.RA9vJ6wS9KTGrFYbiPABlwNTcl8-w3MuvEPUrzz1Rbr90130_provenance
;
np:hasPublicationInfo
dgn-np:NP300981.RA9vJ6wS9KTGrFYbiPABlwNTcl8-w3MuvEPUrzz1Rbr90130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP300981.RA9vJ6wS9KTGrFYbiPABlwNTcl8-w3MuvEPUrzz1Rbr90130_assertion
a
np:Assertion
.
dgn-np:NP300981.RA9vJ6wS9KTGrFYbiPABlwNTcl8-w3MuvEPUrzz1Rbr90130_provenance
a
np:Provenance
.
dgn-np:NP300981.RA9vJ6wS9KTGrFYbiPABlwNTcl8-w3MuvEPUrzz1Rbr90130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP300981.RA9vJ6wS9KTGrFYbiPABlwNTcl8-w3MuvEPUrzz1Rbr90130_assertion
{
miriam-gene:81
a
ncit:C16612
.
lld:C1709661
a
ncit:C7057
.
dgn-gda:DGN9a688b62045ceb551a2b121c8f1b88ab
sio:SIO_000628
miriam-gene:81
,
lld:C1709661
;
a
sio:SIO_001121
.
}
dgn-np:NP300981.RA9vJ6wS9KTGrFYbiPABlwNTcl8-w3MuvEPUrzz1Rbr90130_provenance
{
dgn-np:NP300981.RA9vJ6wS9KTGrFYbiPABlwNTcl8-w3MuvEPUrzz1Rbr90130_assertion
dcterms:description
"[To investigate the promoter mutations of ACTN4 and SYNPO genes in patients with idiopathic focal segmental glomerulosclerosis (FSGS), and to provide functional analysis of these mutations in the role of FSGS occurrence.]. 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:19666657
;
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:NP300981.RA9vJ6wS9KTGrFYbiPABlwNTcl8-w3MuvEPUrzz1Rbr90130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:51+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" .
}