@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP485797.RAdzXiBsNmOSQTJvdBojGq4MXNbF5F0ermPNw3zqtm-FI
> .
@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:NP485797.RAdzXiBsNmOSQTJvdBojGq4MXNbF5F0ermPNw3zqtm-FI130_head
{
this:
np:hasAssertion
dgn-np:NP485797.RAdzXiBsNmOSQTJvdBojGq4MXNbF5F0ermPNw3zqtm-FI130_assertion
;
np:hasProvenance
dgn-np:NP485797.RAdzXiBsNmOSQTJvdBojGq4MXNbF5F0ermPNw3zqtm-FI130_provenance
;
np:hasPublicationInfo
dgn-np:NP485797.RAdzXiBsNmOSQTJvdBojGq4MXNbF5F0ermPNw3zqtm-FI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP485797.RAdzXiBsNmOSQTJvdBojGq4MXNbF5F0ermPNw3zqtm-FI130_assertion
a
np:Assertion
.
dgn-np:NP485797.RAdzXiBsNmOSQTJvdBojGq4MXNbF5F0ermPNw3zqtm-FI130_provenance
a
np:Provenance
.
dgn-np:NP485797.RAdzXiBsNmOSQTJvdBojGq4MXNbF5F0ermPNw3zqtm-FI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP485797.RAdzXiBsNmOSQTJvdBojGq4MXNbF5F0ermPNw3zqtm-FI130_assertion
{
miriam-gene:2138
a
ncit:C16612
.
lld:C0011053
a
ncit:C7057
.
dgn-gda:DGN7903f1f95dbd0b276c320c2d75e49be1
sio:SIO_000628
miriam-gene:2138
,
lld:C0011053
;
a
sio:SIO_001121
.
}
dgn-np:NP485797.RAdzXiBsNmOSQTJvdBojGq4MXNbF5F0ermPNw3zqtm-FI130_provenance
{
dgn-np:NP485797.RAdzXiBsNmOSQTJvdBojGq4MXNbF5F0ermPNw3zqtm-FI130_assertion
dcterms:description
"[Mutation analysis of the PDS gene and the EYA1 gene, which are reported to be responsible for hearing loss associated with ear anomalies, was performed in 24 deaf patients with various middle and inner ear anomalies.]. 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:11558900
;
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:NP485797.RAdzXiBsNmOSQTJvdBojGq4MXNbF5F0ermPNw3zqtm-FI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:50+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" .
}