@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP811586.RAOeR1MUhye94uqeDmoar08Uw1hDZGwG3NiGwELCqTEBg
> .
@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:NP811586.RAOeR1MUhye94uqeDmoar08Uw1hDZGwG3NiGwELCqTEBg130_head
{
this:
np:hasAssertion
dgn-np:NP811586.RAOeR1MUhye94uqeDmoar08Uw1hDZGwG3NiGwELCqTEBg130_assertion
;
np:hasProvenance
dgn-np:NP811586.RAOeR1MUhye94uqeDmoar08Uw1hDZGwG3NiGwELCqTEBg130_provenance
;
np:hasPublicationInfo
dgn-np:NP811586.RAOeR1MUhye94uqeDmoar08Uw1hDZGwG3NiGwELCqTEBg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP811586.RAOeR1MUhye94uqeDmoar08Uw1hDZGwG3NiGwELCqTEBg130_assertion
a
np:Assertion
.
dgn-np:NP811586.RAOeR1MUhye94uqeDmoar08Uw1hDZGwG3NiGwELCqTEBg130_provenance
a
np:Provenance
.
dgn-np:NP811586.RAOeR1MUhye94uqeDmoar08Uw1hDZGwG3NiGwELCqTEBg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP811586.RAOeR1MUhye94uqeDmoar08Uw1hDZGwG3NiGwELCqTEBg130_assertion
{
miriam-gene:4907
a
ncit:C16612
.
lld:C0011053
a
ncit:C7057
.
dgn-gda:DGNa01052b8e81559943464e3bd01de13c0
sio:SIO_000628
miriam-gene:4907
,
lld:C0011053
;
a
sio:SIO_001121
.
}
dgn-np:NP811586.RAOeR1MUhye94uqeDmoar08Uw1hDZGwG3NiGwELCqTEBg130_provenance
{
dgn-np:NP811586.RAOeR1MUhye94uqeDmoar08Uw1hDZGwG3NiGwELCqTEBg130_assertion
dcterms:description
"[This prospective study involved 79 homozygote and heterozygote sickle cell anaemia patients (16 to 50 years old) and a control group of 40 people.All patients underwent ENT, audiological and brainstem auditory evoked responses (BSER) examinations in order to evaluate the incidence of sensorineural hearing loss (SNHL), to identify the changes at the level of the cochlear nerve and the central pathways, and to determine the most vulnerable group, in order to intervene with early prevention and rehabilitation for this condition.A hearing loss of greater than 20 dB at two or more frequencies was found in 36 (45.57 per cent) sickle cell patients (19 (47.22 per cent) HbSC patients and 17 (43.59 per cent) HbSS patients) and three (7.5 per cent) members of the control group.]. 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:16762092
;
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:NP811586.RAOeR1MUhye94uqeDmoar08Uw1hDZGwG3NiGwELCqTEBg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:17+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" .
}