@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP936944.RAB9SCtdd8Sg_ZP7-qgGbYxMpyHVWH5VDTvUyG2chHniA
> .
@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:NP936944.RAB9SCtdd8Sg_ZP7-qgGbYxMpyHVWH5VDTvUyG2chHniA130_head
{
this:
np:hasAssertion
dgn-np:NP936944.RAB9SCtdd8Sg_ZP7-qgGbYxMpyHVWH5VDTvUyG2chHniA130_assertion
;
np:hasProvenance
dgn-np:NP936944.RAB9SCtdd8Sg_ZP7-qgGbYxMpyHVWH5VDTvUyG2chHniA130_provenance
;
np:hasPublicationInfo
dgn-np:NP936944.RAB9SCtdd8Sg_ZP7-qgGbYxMpyHVWH5VDTvUyG2chHniA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP936944.RAB9SCtdd8Sg_ZP7-qgGbYxMpyHVWH5VDTvUyG2chHniA130_assertion
a
np:Assertion
.
dgn-np:NP936944.RAB9SCtdd8Sg_ZP7-qgGbYxMpyHVWH5VDTvUyG2chHniA130_provenance
a
np:Provenance
.
dgn-np:NP936944.RAB9SCtdd8Sg_ZP7-qgGbYxMpyHVWH5VDTvUyG2chHniA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP936944.RAB9SCtdd8Sg_ZP7-qgGbYxMpyHVWH5VDTvUyG2chHniA130_assertion
{
miriam-gene:64072
a
ncit:C16612
.
lld:C3711374
a
ncit:C7057
.
dgn-gda:DGN4c82b4aede3f6807155db54127860db7
sio:SIO_000628
miriam-gene:64072
,
lld:C3711374
;
a
sio:SIO_001122
.
}
dgn-np:NP936944.RAB9SCtdd8Sg_ZP7-qgGbYxMpyHVWH5VDTvUyG2chHniA130_provenance
{
dgn-np:NP936944.RAB9SCtdd8Sg_ZP7-qgGbYxMpyHVWH5VDTvUyG2chHniA130_assertion
dcterms:description
"[Mutations in the human cadherin 23 (CDH23) gene cause deafness, neurosensory, autosomal recessive 12 (DFNB12) nonsyndromic hearing loss or Usher syndrome, type 1D (characterized by hearing impairment, vestibular dysfunction, and visual impairment).]. 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:21689626
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
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 .
}
dgn-np:NP936944.RAB9SCtdd8Sg_ZP7-qgGbYxMpyHVWH5VDTvUyG2chHniA130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:47:12+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}