@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP775384.RA4VISvyLWPlxCMPFJDvY2S3e5eHQ8-jjT0GfSLMIz_b0
> .
@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:NP775384.RA4VISvyLWPlxCMPFJDvY2S3e5eHQ8-jjT0GfSLMIz_b0130_head
{
this:
np:hasAssertion
dgn-np:NP775384.RA4VISvyLWPlxCMPFJDvY2S3e5eHQ8-jjT0GfSLMIz_b0130_assertion
;
np:hasProvenance
dgn-np:NP775384.RA4VISvyLWPlxCMPFJDvY2S3e5eHQ8-jjT0GfSLMIz_b0130_provenance
;
np:hasPublicationInfo
dgn-np:NP775384.RA4VISvyLWPlxCMPFJDvY2S3e5eHQ8-jjT0GfSLMIz_b0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP775384.RA4VISvyLWPlxCMPFJDvY2S3e5eHQ8-jjT0GfSLMIz_b0130_assertion
a
np:Assertion
.
dgn-np:NP775384.RA4VISvyLWPlxCMPFJDvY2S3e5eHQ8-jjT0GfSLMIz_b0130_provenance
a
np:Provenance
.
dgn-np:NP775384.RA4VISvyLWPlxCMPFJDvY2S3e5eHQ8-jjT0GfSLMIz_b0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP775384.RA4VISvyLWPlxCMPFJDvY2S3e5eHQ8-jjT0GfSLMIz_b0130_assertion
{
miriam-gene:7439
a
ncit:C16612
.
lld:C0339510
a
ncit:C7057
.
dgn-gda:DGN7938fc175410fdb095cc1d5273534111
sio:SIO_000628
miriam-gene:7439
,
lld:C0339510
;
a
sio:SIO_001121
.
}
dgn-np:NP775384.RA4VISvyLWPlxCMPFJDvY2S3e5eHQ8-jjT0GfSLMIz_b0130_provenance
{
dgn-np:NP775384.RA4VISvyLWPlxCMPFJDvY2S3e5eHQ8-jjT0GfSLMIz_b0130_assertion
dcterms:description
"[Our results add to the clinical, imaging, and molecular knowledge of Best disease and suggest that OCT can recognize retinal lesions in some asymptomatic carriers of BEST1 mutations as early as 8 years of age.]. 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:21077756
;
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:NP775384.RA4VISvyLWPlxCMPFJDvY2S3e5eHQ8-jjT0GfSLMIz_b0130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:28+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" .
}