@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP122297.RA4xJI0QTDG9sLumkgINC7HfJ-Q3_LLL-AhmRxbUVDnIg
> .
@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:NP122297.RA4xJI0QTDG9sLumkgINC7HfJ-Q3_LLL-AhmRxbUVDnIg130_head
{
this:
np:hasAssertion
dgn-np:NP122297.RA4xJI0QTDG9sLumkgINC7HfJ-Q3_LLL-AhmRxbUVDnIg130_assertion
;
np:hasProvenance
dgn-np:NP122297.RA4xJI0QTDG9sLumkgINC7HfJ-Q3_LLL-AhmRxbUVDnIg130_provenance
;
np:hasPublicationInfo
dgn-np:NP122297.RA4xJI0QTDG9sLumkgINC7HfJ-Q3_LLL-AhmRxbUVDnIg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP122297.RA4xJI0QTDG9sLumkgINC7HfJ-Q3_LLL-AhmRxbUVDnIg130_assertion
a
np:Assertion
.
dgn-np:NP122297.RA4xJI0QTDG9sLumkgINC7HfJ-Q3_LLL-AhmRxbUVDnIg130_provenance
a
np:Provenance
.
dgn-np:NP122297.RA4xJI0QTDG9sLumkgINC7HfJ-Q3_LLL-AhmRxbUVDnIg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP122297.RA4xJI0QTDG9sLumkgINC7HfJ-Q3_LLL-AhmRxbUVDnIg130_assertion
{
miriam-gene:7399
a
ncit:C16612
.
lld:C0035334
a
ncit:C7057
.
dgn-gda:DGN6bfe79319585e8bf276f760fc164c391
sio:SIO_000628
miriam-gene:7399
,
lld:C0035334
;
a
sio:SIO_001122
.
}
dgn-np:NP122297.RA4xJI0QTDG9sLumkgINC7HfJ-Q3_LLL-AhmRxbUVDnIg130_provenance
{
dgn-np:NP122297.RA4xJI0QTDG9sLumkgINC7HfJ-Q3_LLL-AhmRxbUVDnIg130_assertion
dcterms:description
"[Comparative analysis of both phenotypic and genotypic data supports the hypothesis that sensorineural hearing loss in patients with Retinitis Pigmentosa may depend on the nature and on the association of the USH2A allele variants present.]. 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:14970843
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP122297.RA4xJI0QTDG9sLumkgINC7HfJ-Q3_LLL-AhmRxbUVDnIg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:03+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" .
}