@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP550868.RABY4YQx1cdOvijiME261ApPgxJx3DSyggoYTaQqKcGD4
> .
@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:NP550868.RABY4YQx1cdOvijiME261ApPgxJx3DSyggoYTaQqKcGD4130_head
{
this:
np:hasAssertion
dgn-np:NP550868.RABY4YQx1cdOvijiME261ApPgxJx3DSyggoYTaQqKcGD4130_assertion
;
np:hasProvenance
dgn-np:NP550868.RABY4YQx1cdOvijiME261ApPgxJx3DSyggoYTaQqKcGD4130_provenance
;
np:hasPublicationInfo
dgn-np:NP550868.RABY4YQx1cdOvijiME261ApPgxJx3DSyggoYTaQqKcGD4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP550868.RABY4YQx1cdOvijiME261ApPgxJx3DSyggoYTaQqKcGD4130_assertion
a
np:Assertion
.
dgn-np:NP550868.RABY4YQx1cdOvijiME261ApPgxJx3DSyggoYTaQqKcGD4130_provenance
a
np:Provenance
.
dgn-np:NP550868.RABY4YQx1cdOvijiME261ApPgxJx3DSyggoYTaQqKcGD4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP550868.RABY4YQx1cdOvijiME261ApPgxJx3DSyggoYTaQqKcGD4130_assertion
{
miriam-gene:6120
a
ncit:C16612
.
lld:C0035304
a
ncit:C7057
.
dgn-gda:DGN4ac1c6c57be9f7c9ce8d0e430305a9bc
sio:SIO_000628
miriam-gene:6120
,
lld:C0035304
;
a
sio:SIO_001121
.
}
dgn-np:NP550868.RABY4YQx1cdOvijiME261ApPgxJx3DSyggoYTaQqKcGD4130_provenance
{
dgn-np:NP550868.RABY4YQx1cdOvijiME261ApPgxJx3DSyggoYTaQqKcGD4130_assertion
dcterms:description
"[This study demonstrates the potential of gene therapy approaches for the treatment of retinal degenerations caused by defects specific to the RPE and supports the use of lentiviral vectors for the treatment of such disorders.]. 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:15660111
;
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:NP550868.RABY4YQx1cdOvijiME261ApPgxJx3DSyggoYTaQqKcGD4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:32+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" .
}