@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP68414.RAesvQttxwrXmz8My7RkpHl2NHP-5AZ3Pa7HsQ47FAyT8
> .
@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/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@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/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP68414.RAesvQttxwrXmz8My7RkpHl2NHP-5AZ3Pa7HsQ47FAyT8130_head
{
this:
np:hasAssertion
dgn-np:NP68414.RAesvQttxwrXmz8My7RkpHl2NHP-5AZ3Pa7HsQ47FAyT8130_assertion
;
np:hasProvenance
dgn-np:NP68414.RAesvQttxwrXmz8My7RkpHl2NHP-5AZ3Pa7HsQ47FAyT8130_provenance
;
np:hasPublicationInfo
dgn-np:NP68414.RAesvQttxwrXmz8My7RkpHl2NHP-5AZ3Pa7HsQ47FAyT8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP68414.RAesvQttxwrXmz8My7RkpHl2NHP-5AZ3Pa7HsQ47FAyT8130_assertion
a
np:Assertion
.
dgn-np:NP68414.RAesvQttxwrXmz8My7RkpHl2NHP-5AZ3Pa7HsQ47FAyT8130_provenance
a
np:Provenance
.
dgn-np:NP68414.RAesvQttxwrXmz8My7RkpHl2NHP-5AZ3Pa7HsQ47FAyT8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP68414.RAesvQttxwrXmz8My7RkpHl2NHP-5AZ3Pa7HsQ47FAyT8130_assertion
{
miriam-gene:5172
a
ncit:C16612
.
lld:C0018784
a
ncit:C7057
.
dgn-gda:DGNa3fb3c8e4efbc0db6c0c1577ec001628
sio:SIO_000628
miriam-gene:5172
,
lld:C0018784
;
a
sio:SIO_001122
.
}
dgn-np:NP68414.RAesvQttxwrXmz8My7RkpHl2NHP-5AZ3Pa7HsQ47FAyT8130_provenance
{
dgn-np:NP68414.RAesvQttxwrXmz8My7RkpHl2NHP-5AZ3Pa7HsQ47FAyT8130_assertion
dcterms:description
"[To investigate the hot spot mutation of SLC26A4 gene and its incidence among patients with moderate to profound sensorineural hearing loss (SNHL) and to analyze the epidemiology of enlarged vestibular aqueduct syndrome in China.]. 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:18067822
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP68414.RAesvQttxwrXmz8My7RkpHl2NHP-5AZ3Pa7HsQ47FAyT8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:32+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:disgenetrdf
;
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
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}