@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP425675.RArsQ3enThC0qi5hh3wkMu8CTYqJ-rBHBDrADb0dmQyFU
> .
@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:NP425675.RArsQ3enThC0qi5hh3wkMu8CTYqJ-rBHBDrADb0dmQyFU130_head
{
this:
np:hasAssertion
dgn-np:NP425675.RArsQ3enThC0qi5hh3wkMu8CTYqJ-rBHBDrADb0dmQyFU130_assertion
;
np:hasProvenance
dgn-np:NP425675.RArsQ3enThC0qi5hh3wkMu8CTYqJ-rBHBDrADb0dmQyFU130_provenance
;
np:hasPublicationInfo
dgn-np:NP425675.RArsQ3enThC0qi5hh3wkMu8CTYqJ-rBHBDrADb0dmQyFU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP425675.RArsQ3enThC0qi5hh3wkMu8CTYqJ-rBHBDrADb0dmQyFU130_assertion
a
np:Assertion
.
dgn-np:NP425675.RArsQ3enThC0qi5hh3wkMu8CTYqJ-rBHBDrADb0dmQyFU130_provenance
a
np:Provenance
.
dgn-np:NP425675.RArsQ3enThC0qi5hh3wkMu8CTYqJ-rBHBDrADb0dmQyFU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP425675.RArsQ3enThC0qi5hh3wkMu8CTYqJ-rBHBDrADb0dmQyFU130_assertion
{
miriam-gene:1286
a
ncit:C16612
.
lld:C1567741
a
ncit:C7057
.
dgn-gda:DGNb7527540c7d30628cb5d457dd7d346a6
sio:SIO_000628
miriam-gene:1286
,
lld:C1567741
;
a
sio:SIO_001121
.
}
dgn-np:NP425675.RArsQ3enThC0qi5hh3wkMu8CTYqJ-rBHBDrADb0dmQyFU130_provenance
{
dgn-np:NP425675.RArsQ3enThC0qi5hh3wkMu8CTYqJ-rBHBDrADb0dmQyFU130_assertion
dcterms:description
"[It is unclear whether individuals with TBMN and impaired renal function represent part of the spectrum of TBMN associated with heterozygous COL4A3 or COL4A4 mutations, or if their disease is caused by mutations of other genes, or whether it is caused by a second coexistent renal lesion or is misdiagnosed Alport syndrome.]. 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:15880323
;
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:NP425675.RArsQ3enThC0qi5hh3wkMu8CTYqJ-rBHBDrADb0dmQyFU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:12+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" .
}