@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP160548.RAQdhK0mEjNdpcCcZ5u46-_sN0M0cuo0eAIapDo5ozOgM
> .
@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:NP160548.RAQdhK0mEjNdpcCcZ5u46-_sN0M0cuo0eAIapDo5ozOgM130_head
{
this:
np:hasAssertion
dgn-np:NP160548.RAQdhK0mEjNdpcCcZ5u46-_sN0M0cuo0eAIapDo5ozOgM130_assertion
;
np:hasProvenance
dgn-np:NP160548.RAQdhK0mEjNdpcCcZ5u46-_sN0M0cuo0eAIapDo5ozOgM130_provenance
;
np:hasPublicationInfo
dgn-np:NP160548.RAQdhK0mEjNdpcCcZ5u46-_sN0M0cuo0eAIapDo5ozOgM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP160548.RAQdhK0mEjNdpcCcZ5u46-_sN0M0cuo0eAIapDo5ozOgM130_assertion
a
np:Assertion
.
dgn-np:NP160548.RAQdhK0mEjNdpcCcZ5u46-_sN0M0cuo0eAIapDo5ozOgM130_provenance
a
np:Provenance
.
dgn-np:NP160548.RAQdhK0mEjNdpcCcZ5u46-_sN0M0cuo0eAIapDo5ozOgM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP160548.RAQdhK0mEjNdpcCcZ5u46-_sN0M0cuo0eAIapDo5ozOgM130_assertion
{
miriam-gene:3125
a
ncit:C16612
.
lld:C0017668
a
ncit:C7057
.
dgn-gda:DGNee8e2bf930e3c32c197f445031ba1972
sio:SIO_000628
miriam-gene:3125
,
lld:C0017668
;
a
sio:SIO_001121
.
}
dgn-np:NP160548.RAQdhK0mEjNdpcCcZ5u46-_sN0M0cuo0eAIapDo5ozOgM130_provenance
{
dgn-np:NP160548.RAQdhK0mEjNdpcCcZ5u46-_sN0M0cuo0eAIapDo5ozOgM130_assertion
dcterms:description
"[The frequency of this haplotype in the Australian dialysis and transplant population with focal glomerulosclerosis was compared to that seen in the general Australian Caucasian population and was not significantly different suggesting that the presence of the HLA alleles HLA-A1, B8, DR3, DR7 may increase the predisposition to familial glomerulosclerosis but additional factors are required for disease development and progression.]. 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:7503147
;
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:NP160548.RAQdhK0mEjNdpcCcZ5u46-_sN0M0cuo0eAIapDo5ozOgM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:27+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" .
}