@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP764972.RAlZ416lsC0jz1iJu6WZ_gszEuUMyMhreK9-XLzfp01k8
> .
@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:NP764972.RAlZ416lsC0jz1iJu6WZ_gszEuUMyMhreK9-XLzfp01k8130_head
{
this:
np:hasAssertion
dgn-np:NP764972.RAlZ416lsC0jz1iJu6WZ_gszEuUMyMhreK9-XLzfp01k8130_assertion
;
np:hasProvenance
dgn-np:NP764972.RAlZ416lsC0jz1iJu6WZ_gszEuUMyMhreK9-XLzfp01k8130_provenance
;
np:hasPublicationInfo
dgn-np:NP764972.RAlZ416lsC0jz1iJu6WZ_gszEuUMyMhreK9-XLzfp01k8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP764972.RAlZ416lsC0jz1iJu6WZ_gszEuUMyMhreK9-XLzfp01k8130_assertion
a
np:Assertion
.
dgn-np:NP764972.RAlZ416lsC0jz1iJu6WZ_gszEuUMyMhreK9-XLzfp01k8130_provenance
a
np:Provenance
.
dgn-np:NP764972.RAlZ416lsC0jz1iJu6WZ_gszEuUMyMhreK9-XLzfp01k8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP764972.RAlZ416lsC0jz1iJu6WZ_gszEuUMyMhreK9-XLzfp01k8130_assertion
{
miriam-gene:2706
a
ncit:C16612
.
lld:C0037274
a
ncit:C7057
.
dgn-gda:DGN991f793acb0f0c3137ebea7790e9bafb
sio:SIO_000628
miriam-gene:2706
,
lld:C0037274
;
a
sio:SIO_001121
.
}
dgn-np:NP764972.RAlZ416lsC0jz1iJu6WZ_gszEuUMyMhreK9-XLzfp01k8130_provenance
{
dgn-np:NP764972.RAlZ416lsC0jz1iJu6WZ_gszEuUMyMhreK9-XLzfp01k8130_assertion
dcterms:description
"[Knowledge of the PTMs of Cx26 will be instrumental in understanding how alterations in the cellular mechanisms of Cx26 channel biogenesis and function lead to losses in auditory function and disfiguring skin disorders.]. 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:19775242
;
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:NP764972.RAlZ416lsC0jz1iJu6WZ_gszEuUMyMhreK9-XLzfp01k8130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:31+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" .
}