@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP822928.RAjz7Cf2r26elDYXxiik4u8ZdfrEKk_JYdmUt60Oz2TAQ
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP822928.RAjz7Cf2r26elDYXxiik4u8ZdfrEKk_JYdmUt60Oz2TAQ130_head
{
this:
np:hasAssertion
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;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP822928.RAjz7Cf2r26elDYXxiik4u8ZdfrEKk_JYdmUt60Oz2TAQ130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP822928.RAjz7Cf2r26elDYXxiik4u8ZdfrEKk_JYdmUt60Oz2TAQ130_assertion
a
np:Assertion
.
dgn-np:NP822928.RAjz7Cf2r26elDYXxiik4u8ZdfrEKk_JYdmUt60Oz2TAQ130_provenance
a
np:Provenance
.
dgn-np:NP822928.RAjz7Cf2r26elDYXxiik4u8ZdfrEKk_JYdmUt60Oz2TAQ130_publicationInfo
a
np:PublicationInfo
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{
miriam-gene:9414
a
ncit:C16612
.
lld:C0155552
a
ncit:C7057
.
dgn-gda:DGNc332cda18c750f270cdfd1ac9d5ad6e3
sio:SIO_000628
miriam-gene:9414
,
lld:C0155552
;
a
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.
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dgn-np:NP822928.RAjz7Cf2r26elDYXxiik4u8ZdfrEKk_JYdmUt60Oz2TAQ130_provenance
{
dgn-np:NP822928.RAjz7Cf2r26elDYXxiik4u8ZdfrEKk_JYdmUt60Oz2TAQ130_assertion
dcterms:description
"[In the present study, we conducted genetic analyses of the TJP2 and CLDN14 genes in 87 unrelated patients with ADNSHL and 48 unrelated patients with either ARNSHL or potentially sporadic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:24752540
;
prov:wasDerivedFrom
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;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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 .
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dgn-np:NP822928.RAjz7Cf2r26elDYXxiik4u8ZdfrEKk_JYdmUt60Oz2TAQ130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:59+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
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;
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
"v3.0.0.0" .
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pav:version
"v3.0.0" .
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