@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP325998.RAqC9KkAO0Zp1s5krRns8085K64IJid7RSsXtOh1Czp3c
> .
@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:NP325998.RAqC9KkAO0Zp1s5krRns8085K64IJid7RSsXtOh1Czp3c130_head
{
this:
np:hasAssertion
dgn-np:NP325998.RAqC9KkAO0Zp1s5krRns8085K64IJid7RSsXtOh1Czp3c130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP325998.RAqC9KkAO0Zp1s5krRns8085K64IJid7RSsXtOh1Czp3c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP325998.RAqC9KkAO0Zp1s5krRns8085K64IJid7RSsXtOh1Czp3c130_assertion
a
np:Assertion
.
dgn-np:NP325998.RAqC9KkAO0Zp1s5krRns8085K64IJid7RSsXtOh1Czp3c130_provenance
a
np:Provenance
.
dgn-np:NP325998.RAqC9KkAO0Zp1s5krRns8085K64IJid7RSsXtOh1Czp3c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP325998.RAqC9KkAO0Zp1s5krRns8085K64IJid7RSsXtOh1Czp3c130_assertion
{
miriam-gene:1392
a
ncit:C16612
.
lld:C0022661
a
ncit:C7057
.
dgn-gda:DGN388b83e4294eb1af7437791086fb9362
sio:SIO_000628
miriam-gene:1392
,
lld:C0022661
;
a
sio:SIO_001121
.
}
dgn-np:NP325998.RAqC9KkAO0Zp1s5krRns8085K64IJid7RSsXtOh1Czp3c130_provenance
{
dgn-np:NP325998.RAqC9KkAO0Zp1s5krRns8085K64IJid7RSsXtOh1Czp3c130_assertion
dcterms:description
"[Our data confirm for the first time a definite association of heterozygous COL4A3/COL4A4 mutations with familial microscopic haematuria, thin basement membrane nephropathy and the late development of familial proteinuria, CRF, and ESRD, due to FSGS, indicating that the term 'benign familial haematuria' is a misnomer, at least in this cohort.]. 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:19357112
;
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:NP325998.RAqC9KkAO0Zp1s5krRns8085K64IJid7RSsXtOh1Czp3c130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:40:47+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" .
}