@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP51520.RAez5HkF9OXGUm22XhCVveGluXdVxh0erPZqludPBG4zw
> .
@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/v3.0.0/void/
> .
dgn-np:NP51520.RAez5HkF9OXGUm22XhCVveGluXdVxh0erPZqludPBG4zw130_head
{
this:
np:hasAssertion
dgn-np:NP51520.RAez5HkF9OXGUm22XhCVveGluXdVxh0erPZqludPBG4zw130_assertion
;
np:hasProvenance
dgn-np:NP51520.RAez5HkF9OXGUm22XhCVveGluXdVxh0erPZqludPBG4zw130_provenance
;
np:hasPublicationInfo
dgn-np:NP51520.RAez5HkF9OXGUm22XhCVveGluXdVxh0erPZqludPBG4zw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP51520.RAez5HkF9OXGUm22XhCVveGluXdVxh0erPZqludPBG4zw130_assertion
a
np:Assertion
.
dgn-np:NP51520.RAez5HkF9OXGUm22XhCVveGluXdVxh0erPZqludPBG4zw130_provenance
a
np:Provenance
.
dgn-np:NP51520.RAez5HkF9OXGUm22XhCVveGluXdVxh0erPZqludPBG4zw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP51520.RAez5HkF9OXGUm22XhCVveGluXdVxh0erPZqludPBG4zw130_assertion
{
miriam-gene:2706
a
ncit:C16612
.
lld:C0018784
a
ncit:C7057
.
dgn-gda:DGNf6456f6846ecc271942265844815690c
sio:SIO_000628
miriam-gene:2706
,
lld:C0018784
;
a
sio:SIO_001122
.
}
dgn-np:NP51520.RAez5HkF9OXGUm22XhCVveGluXdVxh0erPZqludPBG4zw130_provenance
{
dgn-np:NP51520.RAez5HkF9OXGUm22XhCVveGluXdVxh0erPZqludPBG4zw130_assertion
dcterms:description
"[Ethnicity should be considered when determining the optimal sequence of diagnostic testing for idiopathic congenital sensorineural hearing loss. Asian patients, in particular, should all be screened for mutations in GJB2, especially in the case of mild he]. 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:21042228
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP51520.RAez5HkF9OXGUm22XhCVveGluXdVxh0erPZqludPBG4zw130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:08+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}