@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP149997.RA5hxEFlqH-Narkga_YCD4ntoBlf3McGHppW2NDWjtz8M
> .
@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:NP149997.RA5hxEFlqH-Narkga_YCD4ntoBlf3McGHppW2NDWjtz8M130_head
{
this:
np:hasAssertion
dgn-np:NP149997.RA5hxEFlqH-Narkga_YCD4ntoBlf3McGHppW2NDWjtz8M130_assertion
;
np:hasProvenance
dgn-np:NP149997.RA5hxEFlqH-Narkga_YCD4ntoBlf3McGHppW2NDWjtz8M130_provenance
;
np:hasPublicationInfo
dgn-np:NP149997.RA5hxEFlqH-Narkga_YCD4ntoBlf3McGHppW2NDWjtz8M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP149997.RA5hxEFlqH-Narkga_YCD4ntoBlf3McGHppW2NDWjtz8M130_assertion
a
np:Assertion
.
dgn-np:NP149997.RA5hxEFlqH-Narkga_YCD4ntoBlf3McGHppW2NDWjtz8M130_provenance
a
np:Provenance
.
dgn-np:NP149997.RA5hxEFlqH-Narkga_YCD4ntoBlf3McGHppW2NDWjtz8M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP149997.RA5hxEFlqH-Narkga_YCD4ntoBlf3McGHppW2NDWjtz8M130_assertion
{
miriam-gene:1187
a
ncit:C16612
.
lld:C0004775
a
ncit:C7057
.
dgn-gda:DGNec1ef2b8e96df52263144182957019aa
sio:SIO_000628
miriam-gene:1187
,
lld:C0004775
;
a
sio:SIO_001121
.
}
dgn-np:NP149997.RA5hxEFlqH-Narkga_YCD4ntoBlf3McGHppW2NDWjtz8M130_provenance
{
dgn-np:NP149997.RA5hxEFlqH-Narkga_YCD4ntoBlf3McGHppW2NDWjtz8M130_assertion
dcterms:description
"[Disruption of the gene encoding Barttin, BSND, results in a'double knockout'of the functions of both ClCKA and ClCKB, manifesting as Bartter syndrome type IV with sensorineural deafness and an especially severe salt-losing phenotype.]. 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:18094726
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP149997.RA5hxEFlqH-Narkga_YCD4ntoBlf3McGHppW2NDWjtz8M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:19+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" .
}