@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP765777.RAwgyPCu2AflIbxcqOFgP6Byp4CMluPOtaDPY-LPo4Xn0
> .
@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:NP765777.RAwgyPCu2AflIbxcqOFgP6Byp4CMluPOtaDPY-LPo4Xn0130_head
{
this:
np:hasAssertion
dgn-np:NP765777.RAwgyPCu2AflIbxcqOFgP6Byp4CMluPOtaDPY-LPo4Xn0130_assertion
;
np:hasProvenance
dgn-np:NP765777.RAwgyPCu2AflIbxcqOFgP6Byp4CMluPOtaDPY-LPo4Xn0130_provenance
;
np:hasPublicationInfo
dgn-np:NP765777.RAwgyPCu2AflIbxcqOFgP6Byp4CMluPOtaDPY-LPo4Xn0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP765777.RAwgyPCu2AflIbxcqOFgP6Byp4CMluPOtaDPY-LPo4Xn0130_assertion
a
np:Assertion
.
dgn-np:NP765777.RAwgyPCu2AflIbxcqOFgP6Byp4CMluPOtaDPY-LPo4Xn0130_provenance
a
np:Provenance
.
dgn-np:NP765777.RAwgyPCu2AflIbxcqOFgP6Byp4CMluPOtaDPY-LPo4Xn0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP765777.RAwgyPCu2AflIbxcqOFgP6Byp4CMluPOtaDPY-LPo4Xn0130_assertion
{
miriam-gene:5172
a
ncit:C16612
.
lld:C0155552
a
ncit:C7057
.
dgn-gda:DGNdde282845e7efbe592f61ee57be7b37e
sio:SIO_000628
miriam-gene:5172
,
lld:C0155552
;
a
sio:SIO_001121
.
}
dgn-np:NP765777.RAwgyPCu2AflIbxcqOFgP6Byp4CMluPOtaDPY-LPo4Xn0130_provenance
{
dgn-np:NP765777.RAwgyPCu2AflIbxcqOFgP6Byp4CMluPOtaDPY-LPo4Xn0130_assertion
dcterms:description
"[However, the high incidence of asymmetric, progressive, and fluctuating hearing loss found in the current study indicates that patients with those features should be routinely screened for SLC26A4 mutation in addition to diagnosis of EVA using CT or MRI.]. 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:19786220
;
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:NP765777.RAwgyPCu2AflIbxcqOFgP6Byp4CMluPOtaDPY-LPo4Xn0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:32+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: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" .
}