@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP43570.RAiCIXg5PBsd_vjkcAUlROm4HztwcC3cpBNifDTt6Pt-c
> .
@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 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:NP43570.RAiCIXg5PBsd_vjkcAUlROm4HztwcC3cpBNifDTt6Pt-c130_head
{
this:
np:hasAssertion
dgn-np:NP43570.RAiCIXg5PBsd_vjkcAUlROm4HztwcC3cpBNifDTt6Pt-c130_assertion
;
np:hasProvenance
dgn-np:NP43570.RAiCIXg5PBsd_vjkcAUlROm4HztwcC3cpBNifDTt6Pt-c130_provenance
;
np:hasPublicationInfo
dgn-np:NP43570.RAiCIXg5PBsd_vjkcAUlROm4HztwcC3cpBNifDTt6Pt-c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP43570.RAiCIXg5PBsd_vjkcAUlROm4HztwcC3cpBNifDTt6Pt-c130_assertion
a
np:Assertion
.
dgn-np:NP43570.RAiCIXg5PBsd_vjkcAUlROm4HztwcC3cpBNifDTt6Pt-c130_provenance
a
np:Provenance
.
dgn-np:NP43570.RAiCIXg5PBsd_vjkcAUlROm4HztwcC3cpBNifDTt6Pt-c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP43570.RAiCIXg5PBsd_vjkcAUlROm4HztwcC3cpBNifDTt6Pt-c130_assertion
{
miriam-gene:2706
a
ncit:C16612
.
lld:C0018784
a
ncit:C7057
.
dgn-gda:DGNc6061dc8d40383cd55266dec6722b37f
sio:SIO_000628
miriam-gene:2706
,
lld:C0018784
;
a
sio:SIO_001122
.
}
dgn-np:NP43570.RAiCIXg5PBsd_vjkcAUlROm4HztwcC3cpBNifDTt6Pt-c130_provenance
{
dgn-np:NP43570.RAiCIXg5PBsd_vjkcAUlROm4HztwcC3cpBNifDTt6Pt-c130_assertion
dct:description
"[Most probands have a congenital HL that is stable, symmetrical and without associated manifestations, but the audiometric profile should not be the only criteria for offering mutational screening of DFNB1 because of the observed variability.]. 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:18758381
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP43570.RAiCIXg5PBsd_vjkcAUlROm4HztwcC3cpBNifDTt6Pt-c130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:19+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}