@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP409449.RAvRaJFi6ChV163ks8qii3WCqO3byvebRsHRnsKKHA7vY
> .
@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:NP409449.RAvRaJFi6ChV163ks8qii3WCqO3byvebRsHRnsKKHA7vY130_head
{
this:
np:hasAssertion
dgn-np:NP409449.RAvRaJFi6ChV163ks8qii3WCqO3byvebRsHRnsKKHA7vY130_assertion
;
np:hasProvenance
dgn-np:NP409449.RAvRaJFi6ChV163ks8qii3WCqO3byvebRsHRnsKKHA7vY130_provenance
;
np:hasPublicationInfo
dgn-np:NP409449.RAvRaJFi6ChV163ks8qii3WCqO3byvebRsHRnsKKHA7vY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP409449.RAvRaJFi6ChV163ks8qii3WCqO3byvebRsHRnsKKHA7vY130_assertion
a
np:Assertion
.
dgn-np:NP409449.RAvRaJFi6ChV163ks8qii3WCqO3byvebRsHRnsKKHA7vY130_provenance
a
np:Provenance
.
dgn-np:NP409449.RAvRaJFi6ChV163ks8qii3WCqO3byvebRsHRnsKKHA7vY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP409449.RAvRaJFi6ChV163ks8qii3WCqO3byvebRsHRnsKKHA7vY130_assertion
{
miriam-gene:778
a
ncit:C16612
.
lld:C0028738
a
ncit:C7057
.
dgn-gda:DGN62b06b5b58409968a7da49a16752f206
sio:SIO_000628
miriam-gene:778
,
lld:C0028738
;
a
sio:SIO_001121
.
}
dgn-np:NP409449.RAvRaJFi6ChV163ks8qii3WCqO3byvebRsHRnsKKHA7vY130_provenance
{
dgn-np:NP409449.RAvRaJFi6ChV163ks8qii3WCqO3byvebRsHRnsKKHA7vY130_assertion
dcterms:description
"[Clinically, CORDX3 shares some features with CSNB2 but is distinguishable from CSNB2 in that it is progressive, can begin in adulthood, has no nystagmus or hyperopic refraction, has only low grade astigmatism, and in dark adaptation lacks cone threshold and has small or no elevation of rod threshold.]. 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:16505158
;
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:NP409449.RAvRaJFi6ChV163ks8qii3WCqO3byvebRsHRnsKKHA7vY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:03+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" .
}