@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP377079.RA9SlZVCscGMduNnvRtogvvxs9V1jTE3OhvxLKuEiz21A
> .
@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:NP377079.RA9SlZVCscGMduNnvRtogvvxs9V1jTE3OhvxLKuEiz21A130_head
{
this:
np:hasAssertion
dgn-np:NP377079.RA9SlZVCscGMduNnvRtogvvxs9V1jTE3OhvxLKuEiz21A130_assertion
;
np:hasProvenance
dgn-np:NP377079.RA9SlZVCscGMduNnvRtogvvxs9V1jTE3OhvxLKuEiz21A130_provenance
;
np:hasPublicationInfo
dgn-np:NP377079.RA9SlZVCscGMduNnvRtogvvxs9V1jTE3OhvxLKuEiz21A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP377079.RA9SlZVCscGMduNnvRtogvvxs9V1jTE3OhvxLKuEiz21A130_assertion
a
np:Assertion
.
dgn-np:NP377079.RA9SlZVCscGMduNnvRtogvvxs9V1jTE3OhvxLKuEiz21A130_provenance
a
np:Provenance
.
dgn-np:NP377079.RA9SlZVCscGMduNnvRtogvvxs9V1jTE3OhvxLKuEiz21A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP377079.RA9SlZVCscGMduNnvRtogvvxs9V1jTE3OhvxLKuEiz21A130_assertion
{
miriam-gene:2706
a
ncit:C16612
.
lld:C0003537
a
ncit:C7057
.
dgn-gda:DGN9d4411772e8b3098ce6085d81ec3dd7a
sio:SIO_000628
miriam-gene:2706
,
lld:C0003537
;
a
sio:SIO_001121
.
}
dgn-np:NP377079.RA9SlZVCscGMduNnvRtogvvxs9V1jTE3OhvxLKuEiz21A130_provenance
{
dgn-np:NP377079.RA9SlZVCscGMduNnvRtogvvxs9V1jTE3OhvxLKuEiz21A130_assertion
dcterms:description
"[Eight children with cochlear implants were subjected to genetic testing for GJB2 and underwent the Raven colored progressive matrices test, Rey's auditory verbal learning test, Rey's complex figure test, the standardized language test for aphasia, the picture vocabulary test, and the standardized comprehension test for abstract words.]. 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:16549217
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP377079.RA9SlZVCscGMduNnvRtogvvxs9V1jTE3OhvxLKuEiz21A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:40+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" .
}