@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP588537.RATU_-Lt2BXbhXSytBGgS9Yg2FAo8mpfxsziYvkcfHyz8
> .
@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:NP588537.RATU_-Lt2BXbhXSytBGgS9Yg2FAo8mpfxsziYvkcfHyz8130_head
{
this:
np:hasAssertion
dgn-np:NP588537.RATU_-Lt2BXbhXSytBGgS9Yg2FAo8mpfxsziYvkcfHyz8130_assertion
;
np:hasProvenance
dgn-np:NP588537.RATU_-Lt2BXbhXSytBGgS9Yg2FAo8mpfxsziYvkcfHyz8130_provenance
;
np:hasPublicationInfo
dgn-np:NP588537.RATU_-Lt2BXbhXSytBGgS9Yg2FAo8mpfxsziYvkcfHyz8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP588537.RATU_-Lt2BXbhXSytBGgS9Yg2FAo8mpfxsziYvkcfHyz8130_assertion
a
np:Assertion
.
dgn-np:NP588537.RATU_-Lt2BXbhXSytBGgS9Yg2FAo8mpfxsziYvkcfHyz8130_provenance
a
np:Provenance
.
dgn-np:NP588537.RATU_-Lt2BXbhXSytBGgS9Yg2FAo8mpfxsziYvkcfHyz8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP588537.RATU_-Lt2BXbhXSytBGgS9Yg2FAo8mpfxsziYvkcfHyz8130_assertion
{
miriam-gene:7439
a
ncit:C16612
.
lld:C2745945
a
ncit:C7057
.
dgn-gda:DGNdf456a79536e7812e36b04143f23ad18
sio:SIO_000628
miriam-gene:7439
,
lld:C2745945
;
a
sio:SIO_001121
.
}
dgn-np:NP588537.RATU_-Lt2BXbhXSytBGgS9Yg2FAo8mpfxsziYvkcfHyz8130_provenance
{
dgn-np:NP588537.RATU_-Lt2BXbhXSytBGgS9Yg2FAo8mpfxsziYvkcfHyz8130_assertion
dcterms:description
"[Subclinical Best VMD (absence of both symptoms and funduscopic lesions) in subjects with BEST1 mutation may vary from the absence of any morphologic and functional abnormalities to the presence of specific SD-OCT and EOG changes.]. 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:21436265
;
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:NP588537.RATU_-Lt2BXbhXSytBGgS9Yg2FAo8mpfxsziYvkcfHyz8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:54+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" .
}