@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP913536.RAPo5wkWDz8zthPozXII57NjSsGElnKTuPjG3tlD5NY68
> .
@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:NP913536.RAPo5wkWDz8zthPozXII57NjSsGElnKTuPjG3tlD5NY68130_head
{
this:
np:hasAssertion
dgn-np:NP913536.RAPo5wkWDz8zthPozXII57NjSsGElnKTuPjG3tlD5NY68130_assertion
;
np:hasProvenance
dgn-np:NP913536.RAPo5wkWDz8zthPozXII57NjSsGElnKTuPjG3tlD5NY68130_provenance
;
np:hasPublicationInfo
dgn-np:NP913536.RAPo5wkWDz8zthPozXII57NjSsGElnKTuPjG3tlD5NY68130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP913536.RAPo5wkWDz8zthPozXII57NjSsGElnKTuPjG3tlD5NY68130_assertion
a
np:Assertion
.
dgn-np:NP913536.RAPo5wkWDz8zthPozXII57NjSsGElnKTuPjG3tlD5NY68130_provenance
a
np:Provenance
.
dgn-np:NP913536.RAPo5wkWDz8zthPozXII57NjSsGElnKTuPjG3tlD5NY68130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP913536.RAPo5wkWDz8zthPozXII57NjSsGElnKTuPjG3tlD5NY68130_assertion
{
miriam-gene:4624
a
ncit:C16612
.
lld:C0581883
a
ncit:C7057
.
dgn-gda:DGNac6038f84fa573811008721d72f001d3
sio:SIO_000628
miriam-gene:4624
,
lld:C0581883
;
a
sio:SIO_001121
.
}
dgn-np:NP913536.RAPo5wkWDz8zthPozXII57NjSsGElnKTuPjG3tlD5NY68130_provenance
{
dgn-np:NP913536.RAPo5wkWDz8zthPozXII57NjSsGElnKTuPjG3tlD5NY68130_assertion
dcterms:description
"[This loss of myosin VI function may not allow myosin VI to transport its cargoes appropriately at the base and within the stereocilia, or to anchor the membrane of stereocilia to actin filaments via its cargos, both of which lead to structural changes in the stereocilia of myosin VI-impaired hair cells, and ultimately leading to deafness.]. 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:18833301
;
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:NP913536.RAPo5wkWDz8zthPozXII57NjSsGElnKTuPjG3tlD5NY68130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:20+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" .
}