@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP353909.RAin8FgoRx-lxDCHChdVHwtA3zEvXOxuZ15P8yeY3ZpVE
> .
@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:NP353909.RAin8FgoRx-lxDCHChdVHwtA3zEvXOxuZ15P8yeY3ZpVE130_head
{
this:
np:hasAssertion
dgn-np:NP353909.RAin8FgoRx-lxDCHChdVHwtA3zEvXOxuZ15P8yeY3ZpVE130_assertion
;
np:hasProvenance
dgn-np:NP353909.RAin8FgoRx-lxDCHChdVHwtA3zEvXOxuZ15P8yeY3ZpVE130_provenance
;
np:hasPublicationInfo
dgn-np:NP353909.RAin8FgoRx-lxDCHChdVHwtA3zEvXOxuZ15P8yeY3ZpVE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP353909.RAin8FgoRx-lxDCHChdVHwtA3zEvXOxuZ15P8yeY3ZpVE130_assertion
a
np:Assertion
.
dgn-np:NP353909.RAin8FgoRx-lxDCHChdVHwtA3zEvXOxuZ15P8yeY3ZpVE130_provenance
a
np:Provenance
.
dgn-np:NP353909.RAin8FgoRx-lxDCHChdVHwtA3zEvXOxuZ15P8yeY3ZpVE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP353909.RAin8FgoRx-lxDCHChdVHwtA3zEvXOxuZ15P8yeY3ZpVE130_assertion
{
miriam-gene:2706
a
ncit:C16612
.
lld:C3711374
a
ncit:C7057
.
dgn-gda:DGNda1655bf9cf497e4c43d716a66a85c5a
sio:SIO_000628
miriam-gene:2706
,
lld:C3711374
;
a
sio:SIO_001122
.
}
dgn-np:NP353909.RAin8FgoRx-lxDCHChdVHwtA3zEvXOxuZ15P8yeY3ZpVE130_provenance
{
dgn-np:NP353909.RAin8FgoRx-lxDCHChdVHwtA3zEvXOxuZ15P8yeY3ZpVE130_assertion
dcterms:description
"[Data from both linkage and heterogeneity analyses on 36 selected autosomal recessive nonsyndromic deafness (RNSD) families, all previously excluded by mutational analysis from GJB2 (Cx26), the leading cause of nonsyndromic deafness, showed no evidence of DFNB2 within the sample.]. 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:11992483
;
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:NP353909.RAin8FgoRx-lxDCHChdVHwtA3zEvXOxuZ15P8yeY3ZpVE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:25+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" .
}