@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP903398.RA-NlJNBb00kUiTX0ocRiAePPviu1be1pBi9BvxNLNibI
> .
@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:NP903398.RA-NlJNBb00kUiTX0ocRiAePPviu1be1pBi9BvxNLNibI130_head
{
this:
np:hasAssertion
dgn-np:NP903398.RA-NlJNBb00kUiTX0ocRiAePPviu1be1pBi9BvxNLNibI130_assertion
;
np:hasProvenance
dgn-np:NP903398.RA-NlJNBb00kUiTX0ocRiAePPviu1be1pBi9BvxNLNibI130_provenance
;
np:hasPublicationInfo
dgn-np:NP903398.RA-NlJNBb00kUiTX0ocRiAePPviu1be1pBi9BvxNLNibI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP903398.RA-NlJNBb00kUiTX0ocRiAePPviu1be1pBi9BvxNLNibI130_assertion
a
np:Assertion
.
dgn-np:NP903398.RA-NlJNBb00kUiTX0ocRiAePPviu1be1pBi9BvxNLNibI130_provenance
a
np:Provenance
.
dgn-np:NP903398.RA-NlJNBb00kUiTX0ocRiAePPviu1be1pBi9BvxNLNibI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP903398.RA-NlJNBb00kUiTX0ocRiAePPviu1be1pBi9BvxNLNibI130_assertion
{
miriam-gene:60498
a
ncit:C16612
.
lld:C0004775
a
ncit:C7057
.
dgn-gda:DGNc2eabb6d4be04536369811e1ba75216a
sio:SIO_000628
miriam-gene:60498
,
lld:C0004775
;
a
sio:SIO_001121
.
}
dgn-np:NP903398.RA-NlJNBb00kUiTX0ocRiAePPviu1be1pBi9BvxNLNibI130_provenance
{
dgn-np:NP903398.RA-NlJNBb00kUiTX0ocRiAePPviu1be1pBi9BvxNLNibI130_assertion
dcterms:description
"[This article will summarize how these new findings have expanded our understanding of whether diseases are homogeneous or heterogeneous entities (Bartter's syndrome versus Gitelman's syndrome), the medical basis of certain diseases of unclear etiology (enuresis), and the nature of risk factors for disease occurrence or progression (IgA nephropathy, chronic renal failure, and hemolytic uremic 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:9203198
;
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:NP903398.RA-NlJNBb00kUiTX0ocRiAePPviu1be1pBi9BvxNLNibI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:15+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" .
}