@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP548597.RAD-3bsh8jGkAIauE7QpkwmqbUuAkQUEdeA_aDrF9JD8s
> .
@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:NP548597.RAD-3bsh8jGkAIauE7QpkwmqbUuAkQUEdeA_aDrF9JD8s130_head
{
this:
np:hasAssertion
dgn-np:NP548597.RAD-3bsh8jGkAIauE7QpkwmqbUuAkQUEdeA_aDrF9JD8s130_assertion
;
np:hasProvenance
dgn-np:NP548597.RAD-3bsh8jGkAIauE7QpkwmqbUuAkQUEdeA_aDrF9JD8s130_provenance
;
np:hasPublicationInfo
dgn-np:NP548597.RAD-3bsh8jGkAIauE7QpkwmqbUuAkQUEdeA_aDrF9JD8s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP548597.RAD-3bsh8jGkAIauE7QpkwmqbUuAkQUEdeA_aDrF9JD8s130_assertion
a
np:Assertion
.
dgn-np:NP548597.RAD-3bsh8jGkAIauE7QpkwmqbUuAkQUEdeA_aDrF9JD8s130_provenance
a
np:Provenance
.
dgn-np:NP548597.RAD-3bsh8jGkAIauE7QpkwmqbUuAkQUEdeA_aDrF9JD8s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP548597.RAD-3bsh8jGkAIauE7QpkwmqbUuAkQUEdeA_aDrF9JD8s130_assertion
{
miriam-gene:2739
a
ncit:C16612
.
lld:C0403396
a
ncit:C7057
.
dgn-gda:DGN09ec85d236b699422116f448172a5972
sio:SIO_000628
miriam-gene:2739
,
lld:C0403396
;
a
sio:SIO_001121
.
}
dgn-np:NP548597.RAD-3bsh8jGkAIauE7QpkwmqbUuAkQUEdeA_aDrF9JD8s130_provenance
{
dgn-np:NP548597.RAD-3bsh8jGkAIauE7QpkwmqbUuAkQUEdeA_aDrF9JD8s130_assertion
dcterms:description
"[To determine whether steroid-sensitive nephrotic syndrome is associated with greater than expected frequencies of specific extended haplotypes of the major histocompatibility complex, we studied genetic markers (Class I, II, III HLA alleles and glyoxalase I) in 173 subjects in 42 families of patients with nephrotic syndrome of childhood.]. 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:1974661
;
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:NP548597.RAD-3bsh8jGkAIauE7QpkwmqbUuAkQUEdeA_aDrF9JD8s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:30+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" .
}