@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP584583.RAOw1lylnj_DKOBUE4c1vJ0XDdUA8r7KNCvFUFj6ZEK4g
> .
@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:NP584583.RAOw1lylnj_DKOBUE4c1vJ0XDdUA8r7KNCvFUFj6ZEK4g130_head
{
this:
np:hasAssertion
dgn-np:NP584583.RAOw1lylnj_DKOBUE4c1vJ0XDdUA8r7KNCvFUFj6ZEK4g130_assertion
;
np:hasProvenance
dgn-np:NP584583.RAOw1lylnj_DKOBUE4c1vJ0XDdUA8r7KNCvFUFj6ZEK4g130_provenance
;
np:hasPublicationInfo
dgn-np:NP584583.RAOw1lylnj_DKOBUE4c1vJ0XDdUA8r7KNCvFUFj6ZEK4g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP584583.RAOw1lylnj_DKOBUE4c1vJ0XDdUA8r7KNCvFUFj6ZEK4g130_assertion
a
np:Assertion
.
dgn-np:NP584583.RAOw1lylnj_DKOBUE4c1vJ0XDdUA8r7KNCvFUFj6ZEK4g130_provenance
a
np:Provenance
.
dgn-np:NP584583.RAOw1lylnj_DKOBUE4c1vJ0XDdUA8r7KNCvFUFj6ZEK4g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP584583.RAOw1lylnj_DKOBUE4c1vJ0XDdUA8r7KNCvFUFj6ZEK4g130_assertion
{
miriam-gene:100861440
a
ncit:C16612
.
lld:C0004775
a
ncit:C7057
.
dgn-gda:DGNe704c94c179d9170fd753ab613596bb6
sio:SIO_000628
miriam-gene:100861440
,
lld:C0004775
;
a
sio:SIO_001121
.
}
dgn-np:NP584583.RAOw1lylnj_DKOBUE4c1vJ0XDdUA8r7KNCvFUFj6ZEK4g130_provenance
{
dgn-np:NP584583.RAOw1lylnj_DKOBUE4c1vJ0XDdUA8r7KNCvFUFj6ZEK4g130_assertion
dcterms:description
"[Of the 125 genes within the DFNB96 interval, the previously identified ARNSHI gene for DFNB36, ESPN, and two genes that cause Bartter syndrome, CLCNKA and CLCNKB, were sequenced, but no potentially causal variants were identified.]. 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:21937999
;
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:NP584583.RAOw1lylnj_DKOBUE4c1vJ0XDdUA8r7KNCvFUFj6ZEK4g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:52+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" .
}