@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP934675.RA95Bs-pm0wh8-QnblvA-uPN5Qrz3Y8RcQtdhHOl6MmxA
> .
@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/v4.0.0/void/
> .
dgn-np:NP934675.RA95Bs-pm0wh8-QnblvA-uPN5Qrz3Y8RcQtdhHOl6MmxA130_head
{
this:
np:hasAssertion
dgn-np:NP934675.RA95Bs-pm0wh8-QnblvA-uPN5Qrz3Y8RcQtdhHOl6MmxA130_assertion
;
np:hasProvenance
dgn-np:NP934675.RA95Bs-pm0wh8-QnblvA-uPN5Qrz3Y8RcQtdhHOl6MmxA130_provenance
;
np:hasPublicationInfo
dgn-np:NP934675.RA95Bs-pm0wh8-QnblvA-uPN5Qrz3Y8RcQtdhHOl6MmxA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP934675.RA95Bs-pm0wh8-QnblvA-uPN5Qrz3Y8RcQtdhHOl6MmxA130_assertion
a
np:Assertion
.
dgn-np:NP934675.RA95Bs-pm0wh8-QnblvA-uPN5Qrz3Y8RcQtdhHOl6MmxA130_provenance
a
np:Provenance
.
dgn-np:NP934675.RA95Bs-pm0wh8-QnblvA-uPN5Qrz3Y8RcQtdhHOl6MmxA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP934675.RA95Bs-pm0wh8-QnblvA-uPN5Qrz3Y8RcQtdhHOl6MmxA130_assertion
{
miriam-gene:2706
a
ncit:C16612
.
lld:C0018784
a
ncit:C7057
.
dgn-gda:DGN6f8691f0f40327bf067e92d33ca3a761
sio:SIO_000628
miriam-gene:2706
,
lld:C0018784
;
a
sio:SIO_001121
.
}
dgn-np:NP934675.RA95Bs-pm0wh8-QnblvA-uPN5Qrz3Y8RcQtdhHOl6MmxA130_provenance
{
dgn-np:NP934675.RA95Bs-pm0wh8-QnblvA-uPN5Qrz3Y8RcQtdhHOl6MmxA130_assertion
dcterms:description
"[In conclusion, this study determines the importance of connexin 26 mutations in Bulgarian children with severe to profound congenital nonsyndromic sensorineural hearing loss, the prevalence of the different mutation variants and their relationship with the ethnical background of the patients.]. 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:22037723
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP934675.RA95Bs-pm0wh8-QnblvA-uPN5Qrz3Y8RcQtdhHOl6MmxA130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:48+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}