@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP528081.RA3ZCtYvSaLgFDto0JeVUkewjXpFi2CL40WYj52Su8Zb4
> .
@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:NP528081.RA3ZCtYvSaLgFDto0JeVUkewjXpFi2CL40WYj52Su8Zb4130_head
{
this:
np:hasAssertion
dgn-np:NP528081.RA3ZCtYvSaLgFDto0JeVUkewjXpFi2CL40WYj52Su8Zb4130_assertion
;
np:hasProvenance
dgn-np:NP528081.RA3ZCtYvSaLgFDto0JeVUkewjXpFi2CL40WYj52Su8Zb4130_provenance
;
np:hasPublicationInfo
dgn-np:NP528081.RA3ZCtYvSaLgFDto0JeVUkewjXpFi2CL40WYj52Su8Zb4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP528081.RA3ZCtYvSaLgFDto0JeVUkewjXpFi2CL40WYj52Su8Zb4130_assertion
a
np:Assertion
.
dgn-np:NP528081.RA3ZCtYvSaLgFDto0JeVUkewjXpFi2CL40WYj52Su8Zb4130_provenance
a
np:Provenance
.
dgn-np:NP528081.RA3ZCtYvSaLgFDto0JeVUkewjXpFi2CL40WYj52Su8Zb4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP528081.RA3ZCtYvSaLgFDto0JeVUkewjXpFi2CL40WYj52Su8Zb4130_assertion
{
miriam-gene:50617
a
ncit:C16612
.
lld:C0018784
a
ncit:C7057
.
dgn-gda:DGNd467f04971d8bba24095430fd19f5138
sio:SIO_000628
miriam-gene:50617
,
lld:C0018784
;
a
sio:SIO_001121
.
}
dgn-np:NP528081.RA3ZCtYvSaLgFDto0JeVUkewjXpFi2CL40WYj52Su8Zb4130_provenance
{
dgn-np:NP528081.RA3ZCtYvSaLgFDto0JeVUkewjXpFi2CL40WYj52Su8Zb4130_assertion
dcterms:description
"[Our study confirms the association of EVA and mutations in the ATP6V1B1 gene and demonstrates that mutations in the ATP6V0A4 gene can also be associated with EVA probably only when the SNHL has an early onset.]. 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:19639346
;
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:NP528081.RA3ZCtYvSaLgFDto0JeVUkewjXpFi2CL40WYj52Su8Zb4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:19+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" .
}