@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP392300.RAN0otIWK7I0HN4BTFKlXX_KPcLIswM5TYmJXbsWaa8cs
> .
@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:NP392300.RAN0otIWK7I0HN4BTFKlXX_KPcLIswM5TYmJXbsWaa8cs130_head
{
this:
np:hasAssertion
dgn-np:NP392300.RAN0otIWK7I0HN4BTFKlXX_KPcLIswM5TYmJXbsWaa8cs130_assertion
;
np:hasProvenance
dgn-np:NP392300.RAN0otIWK7I0HN4BTFKlXX_KPcLIswM5TYmJXbsWaa8cs130_provenance
;
np:hasPublicationInfo
dgn-np:NP392300.RAN0otIWK7I0HN4BTFKlXX_KPcLIswM5TYmJXbsWaa8cs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP392300.RAN0otIWK7I0HN4BTFKlXX_KPcLIswM5TYmJXbsWaa8cs130_assertion
a
np:Assertion
.
dgn-np:NP392300.RAN0otIWK7I0HN4BTFKlXX_KPcLIswM5TYmJXbsWaa8cs130_provenance
a
np:Provenance
.
dgn-np:NP392300.RAN0otIWK7I0HN4BTFKlXX_KPcLIswM5TYmJXbsWaa8cs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP392300.RAN0otIWK7I0HN4BTFKlXX_KPcLIswM5TYmJXbsWaa8cs130_assertion
{
miriam-gene:115861
a
ncit:C16612
.
lld:C0456909
a
ncit:C7057
.
dgn-gda:DGN0dc724a2a273ea7d33b21eae94f5ee68
sio:SIO_000628
miriam-gene:115861
,
lld:C0456909
;
a
sio:SIO_001121
.
}
dgn-np:NP392300.RAN0otIWK7I0HN4BTFKlXX_KPcLIswM5TYmJXbsWaa8cs130_provenance
{
dgn-np:NP392300.RAN0otIWK7I0HN4BTFKlXX_KPcLIswM5TYmJXbsWaa8cs130_assertion
dcterms:description
"[Based upon these results, we propose an alternative therapeutic strategy aimed at recapitulating RdCVF expression in the inner retina, where cell loss is not significant, to prevent secondary cone death and central vision loss in patients suffering from retinitis pigmentosa.]. 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:19843539
;
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:NP392300.RAN0otIWK7I0HN4BTFKlXX_KPcLIswM5TYmJXbsWaa8cs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:53+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" .
}