@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP588738.RA0fYl2Iogxeej67r9jNACZtQI8pU1SL6jcqmBSKmVDGQ
> .
@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:NP588738.RA0fYl2Iogxeej67r9jNACZtQI8pU1SL6jcqmBSKmVDGQ130_head
{
this:
np:hasAssertion
dgn-np:NP588738.RA0fYl2Iogxeej67r9jNACZtQI8pU1SL6jcqmBSKmVDGQ130_assertion
;
np:hasProvenance
dgn-np:NP588738.RA0fYl2Iogxeej67r9jNACZtQI8pU1SL6jcqmBSKmVDGQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP588738.RA0fYl2Iogxeej67r9jNACZtQI8pU1SL6jcqmBSKmVDGQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP588738.RA0fYl2Iogxeej67r9jNACZtQI8pU1SL6jcqmBSKmVDGQ130_assertion
a
np:Assertion
.
dgn-np:NP588738.RA0fYl2Iogxeej67r9jNACZtQI8pU1SL6jcqmBSKmVDGQ130_provenance
a
np:Provenance
.
dgn-np:NP588738.RA0fYl2Iogxeej67r9jNACZtQI8pU1SL6jcqmBSKmVDGQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP588738.RA0fYl2Iogxeej67r9jNACZtQI8pU1SL6jcqmBSKmVDGQ130_assertion
{
miriam-gene:2706
a
ncit:C16612
.
lld:C0155552
a
ncit:C7057
.
dgn-gda:DGNd8ec4aec299827fe280fbf5b95316632
sio:SIO_000628
miriam-gene:2706
,
lld:C0155552
;
a
sio:SIO_001121
.
}
dgn-np:NP588738.RA0fYl2Iogxeej67r9jNACZtQI8pU1SL6jcqmBSKmVDGQ130_provenance
{
dgn-np:NP588738.RA0fYl2Iogxeej67r9jNACZtQI8pU1SL6jcqmBSKmVDGQ130_assertion
dcterms:description
"[Based on these data, we hypothesize that Cx26 profound hearing loss may be not always congenital, with the possibility of an early window of functional time before the final defect is established.]. 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:17222463
;
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:NP588738.RA0fYl2Iogxeej67r9jNACZtQI8pU1SL6jcqmBSKmVDGQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:12+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}