@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP636384.RA6imjwm5RDSQ1JsnzrtTjhw6S9npj5kTL6GMI-M0gX_E
> .
@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:NP636384.RA6imjwm5RDSQ1JsnzrtTjhw6S9npj5kTL6GMI-M0gX_E130_head
{
this:
np:hasAssertion
dgn-np:NP636384.RA6imjwm5RDSQ1JsnzrtTjhw6S9npj5kTL6GMI-M0gX_E130_assertion
;
np:hasProvenance
dgn-np:NP636384.RA6imjwm5RDSQ1JsnzrtTjhw6S9npj5kTL6GMI-M0gX_E130_provenance
;
np:hasPublicationInfo
dgn-np:NP636384.RA6imjwm5RDSQ1JsnzrtTjhw6S9npj5kTL6GMI-M0gX_E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP636384.RA6imjwm5RDSQ1JsnzrtTjhw6S9npj5kTL6GMI-M0gX_E130_assertion
a
np:Assertion
.
dgn-np:NP636384.RA6imjwm5RDSQ1JsnzrtTjhw6S9npj5kTL6GMI-M0gX_E130_provenance
a
np:Provenance
.
dgn-np:NP636384.RA6imjwm5RDSQ1JsnzrtTjhw6S9npj5kTL6GMI-M0gX_E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP636384.RA6imjwm5RDSQ1JsnzrtTjhw6S9npj5kTL6GMI-M0gX_E130_assertion
{
miriam-gene:1351
a
ncit:C16612
.
lld:C0011053
a
ncit:C7057
.
dgn-gda:DGN156d4edd0c66e5ae1195fbce42acac45
sio:SIO_000628
miriam-gene:1351
,
lld:C0011053
;
a
sio:SIO_001121
.
}
dgn-np:NP636384.RA6imjwm5RDSQ1JsnzrtTjhw6S9npj5kTL6GMI-M0gX_E130_provenance
{
dgn-np:NP636384.RA6imjwm5RDSQ1JsnzrtTjhw6S9npj5kTL6GMI-M0gX_E130_assertion
dcterms:description
"[Inclusion criteria for this study were hearing loss of more than 30 dB hearing level affecting at least 3 contiguous frequencies, normal hearing on the contralateral ear, negative history of hearing loss or ear surgery in the affected ear, and magnetic resonance with gadolinium negative for VIII cranial nerve pathologic findings.]. 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:18401280
;
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:NP636384.RA6imjwm5RDSQ1JsnzrtTjhw6S9npj5kTL6GMI-M0gX_E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:24+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" .
}