@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP954503.RAK-7weH_3tH6fGHPPemsQhLQkBSC2yllTezAJVRLC0FI
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP954503.RAK-7weH_3tH6fGHPPemsQhLQkBSC2yllTezAJVRLC0FI130_head
{
this:
np:hasAssertion
dgn-np:NP954503.RAK-7weH_3tH6fGHPPemsQhLQkBSC2yllTezAJVRLC0FI130_assertion
;
np:hasProvenance
dgn-np:NP954503.RAK-7weH_3tH6fGHPPemsQhLQkBSC2yllTezAJVRLC0FI130_provenance
;
np:hasPublicationInfo
dgn-np:NP954503.RAK-7weH_3tH6fGHPPemsQhLQkBSC2yllTezAJVRLC0FI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP954503.RAK-7weH_3tH6fGHPPemsQhLQkBSC2yllTezAJVRLC0FI130_assertion
a
np:Assertion
.
dgn-np:NP954503.RAK-7weH_3tH6fGHPPemsQhLQkBSC2yllTezAJVRLC0FI130_provenance
a
np:Provenance
.
dgn-np:NP954503.RAK-7weH_3tH6fGHPPemsQhLQkBSC2yllTezAJVRLC0FI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP954503.RAK-7weH_3tH6fGHPPemsQhLQkBSC2yllTezAJVRLC0FI130_assertion
{
miriam-gene:84059
a
ncit:C16612
.
lld:C0155552
a
ncit:C7057
.
dgn-gda:DGN963f6492e44ff847802a7a356e392822
sio:SIO_000628
miriam-gene:84059
,
lld:C0155552
;
a
sio:SIO_001121
.
}
dgn-np:NP954503.RAK-7weH_3tH6fGHPPemsQhLQkBSC2yllTezAJVRLC0FI130_provenance
{
dgn-np:NP954503.RAK-7weH_3tH6fGHPPemsQhLQkBSC2yllTezAJVRLC0FI130_assertion
dcterms:description
"[Knock-out and mutation mouse models show that loss of Vlgr1 function leads to abnormal stereociliary development and hearing loss, indicating crucial roles of Vlgr1 in hearing transduction or auditory system development.]. 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:23180093
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP954503.RAK-7weH_3tH6fGHPPemsQhLQkBSC2yllTezAJVRLC0FI130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:47:23+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}