@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP66049.RA_1l7JzX4mFHX8br7k6-zwVDZV5aWRO_wzWiKCZa3fh0
> .
@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:NP66049.RA_1l7JzX4mFHX8br7k6-zwVDZV5aWRO_wzWiKCZa3fh0130_head
{
this:
np:hasAssertion
dgn-np:NP66049.RA_1l7JzX4mFHX8br7k6-zwVDZV5aWRO_wzWiKCZa3fh0130_assertion
;
np:hasProvenance
dgn-np:NP66049.RA_1l7JzX4mFHX8br7k6-zwVDZV5aWRO_wzWiKCZa3fh0130_provenance
;
np:hasPublicationInfo
dgn-np:NP66049.RA_1l7JzX4mFHX8br7k6-zwVDZV5aWRO_wzWiKCZa3fh0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP66049.RA_1l7JzX4mFHX8br7k6-zwVDZV5aWRO_wzWiKCZa3fh0130_assertion
a
np:Assertion
.
dgn-np:NP66049.RA_1l7JzX4mFHX8br7k6-zwVDZV5aWRO_wzWiKCZa3fh0130_provenance
a
np:Provenance
.
dgn-np:NP66049.RA_1l7JzX4mFHX8br7k6-zwVDZV5aWRO_wzWiKCZa3fh0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP66049.RA_1l7JzX4mFHX8br7k6-zwVDZV5aWRO_wzWiKCZa3fh0130_assertion
{
miriam-gene:4868
a
ncit:C16612
.
lld:C0027726
a
ncit:C7057
.
dgn-gda:DGN1ff333b95dfe173293ce339a8197b6c3
sio:SIO_000628
miriam-gene:4868
,
lld:C0027726
;
a
sio:SIO_001122
.
}
dgn-np:NP66049.RA_1l7JzX4mFHX8br7k6-zwVDZV5aWRO_wzWiKCZa3fh0130_provenance
{
dgn-np:NP66049.RA_1l7JzX4mFHX8br7k6-zwVDZV5aWRO_wzWiKCZa3fh0130_assertion
dcterms:description
"[The results demonstrate that NPHS1 and NPHS2 mutations are also present in Chinese sporadic NS patients, suggesting that genetic changes of nephrin and podocin may play pathogenetic roles in some patients with sporadic steroid resistant NS.]. 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:17211152
;
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:NP66049.RA_1l7JzX4mFHX8br7k6-zwVDZV5aWRO_wzWiKCZa3fh0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:31+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" .
}