@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP150509.RADFXJfV6TwW4l2S1OrbidsSU_b4ok6LREtbVFq3JYGwg
> .
@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:NP150509.RADFXJfV6TwW4l2S1OrbidsSU_b4ok6LREtbVFq3JYGwg130_head
{
this:
np:hasAssertion
dgn-np:NP150509.RADFXJfV6TwW4l2S1OrbidsSU_b4ok6LREtbVFq3JYGwg130_assertion
;
np:hasProvenance
dgn-np:NP150509.RADFXJfV6TwW4l2S1OrbidsSU_b4ok6LREtbVFq3JYGwg130_provenance
;
np:hasPublicationInfo
dgn-np:NP150509.RADFXJfV6TwW4l2S1OrbidsSU_b4ok6LREtbVFq3JYGwg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP150509.RADFXJfV6TwW4l2S1OrbidsSU_b4ok6LREtbVFq3JYGwg130_assertion
a
np:Assertion
.
dgn-np:NP150509.RADFXJfV6TwW4l2S1OrbidsSU_b4ok6LREtbVFq3JYGwg130_provenance
a
np:Provenance
.
dgn-np:NP150509.RADFXJfV6TwW4l2S1OrbidsSU_b4ok6LREtbVFq3JYGwg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP150509.RADFXJfV6TwW4l2S1OrbidsSU_b4ok6LREtbVFq3JYGwg130_assertion
{
miriam-gene:6052
a
ncit:C16612
.
lld:C1384666
a
ncit:C7057
.
dgn-gda:DGN18b08e63566c3f81c28055cb57da3219
sio:SIO_000628
miriam-gene:6052
,
lld:C1384666
;
a
sio:SIO_001122
.
}
dgn-np:NP150509.RADFXJfV6TwW4l2S1OrbidsSU_b4ok6LREtbVFq3JYGwg130_provenance
{
dgn-np:NP150509.RADFXJfV6TwW4l2S1OrbidsSU_b4ok6LREtbVFq3JYGwg130_assertion
dcterms:description
"[The prevalence of 12S rRNA mutations related to aminoglycoside ototoxicity in our study population was approximately one percent. Most patients with this mutation and aminoglycoside exposure showed no evidence of hearing loss. Low birth weight was one ris]. 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:20416460
;
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:NP150509.RADFXJfV6TwW4l2S1OrbidsSU_b4ok6LREtbVFq3JYGwg130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:39:05+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" .
}