@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP382403.RAjLRixCDLzNwWInr7ce61_LeDiSYkeCr3CApNeG5mHY4
> .
@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:NP382403.RAjLRixCDLzNwWInr7ce61_LeDiSYkeCr3CApNeG5mHY4130_head
{
this:
np:hasAssertion
dgn-np:NP382403.RAjLRixCDLzNwWInr7ce61_LeDiSYkeCr3CApNeG5mHY4130_assertion
;
np:hasProvenance
dgn-np:NP382403.RAjLRixCDLzNwWInr7ce61_LeDiSYkeCr3CApNeG5mHY4130_provenance
;
np:hasPublicationInfo
dgn-np:NP382403.RAjLRixCDLzNwWInr7ce61_LeDiSYkeCr3CApNeG5mHY4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP382403.RAjLRixCDLzNwWInr7ce61_LeDiSYkeCr3CApNeG5mHY4130_assertion
a
np:Assertion
.
dgn-np:NP382403.RAjLRixCDLzNwWInr7ce61_LeDiSYkeCr3CApNeG5mHY4130_provenance
a
np:Provenance
.
dgn-np:NP382403.RAjLRixCDLzNwWInr7ce61_LeDiSYkeCr3CApNeG5mHY4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP382403.RAjLRixCDLzNwWInr7ce61_LeDiSYkeCr3CApNeG5mHY4130_assertion
{
miriam-gene:2706
a
ncit:C16612
.
lld:C0018784
a
ncit:C7057
.
dgn-gda:DGNf2fb59557e5d091154f31b32a4efb90a
sio:SIO_000628
miriam-gene:2706
,
lld:C0018784
;
a
sio:SIO_001122
.
}
dgn-np:NP382403.RAjLRixCDLzNwWInr7ce61_LeDiSYkeCr3CApNeG5mHY4130_provenance
{
dgn-np:NP382403.RAjLRixCDLzNwWInr7ce61_LeDiSYkeCr3CApNeG5mHY4130_assertion
dcterms:description
"[Further studies are required to determine the exact mechanism by which mutant (V84L), (V95M), and (R143W) Cx26 proteins, which are capable of forming functional homotypic junctional channels in N2A cells, cause the cochlear dysfunction and sensorineural deafness.]. 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:12562518
;
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:NP382403.RAjLRixCDLzNwWInr7ce61_LeDiSYkeCr3CApNeG5mHY4130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:38+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" .
}