@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP930126.RARR8S7F-Nc4Oazb-2ivaxIcz_lb7lFotxoLYPTXW8OmA
> .
@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:NP930126.RARR8S7F-Nc4Oazb-2ivaxIcz_lb7lFotxoLYPTXW8OmA130_head
{
this:
np:hasAssertion
dgn-np:NP930126.RARR8S7F-Nc4Oazb-2ivaxIcz_lb7lFotxoLYPTXW8OmA130_assertion
;
np:hasProvenance
dgn-np:NP930126.RARR8S7F-Nc4Oazb-2ivaxIcz_lb7lFotxoLYPTXW8OmA130_provenance
;
np:hasPublicationInfo
dgn-np:NP930126.RARR8S7F-Nc4Oazb-2ivaxIcz_lb7lFotxoLYPTXW8OmA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP930126.RARR8S7F-Nc4Oazb-2ivaxIcz_lb7lFotxoLYPTXW8OmA130_assertion
a
np:Assertion
.
dgn-np:NP930126.RARR8S7F-Nc4Oazb-2ivaxIcz_lb7lFotxoLYPTXW8OmA130_provenance
a
np:Provenance
.
dgn-np:NP930126.RARR8S7F-Nc4Oazb-2ivaxIcz_lb7lFotxoLYPTXW8OmA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP930126.RARR8S7F-Nc4Oazb-2ivaxIcz_lb7lFotxoLYPTXW8OmA130_assertion
{
miriam-gene:6121
a
ncit:C16612
.
lld:C0035309
a
ncit:C7057
.
dgn-gda:DGN2edec6d6a6221858dbb3aed32d62f36c
sio:SIO_000628
miriam-gene:6121
,
lld:C0035309
;
a
sio:SIO_001121
.
}
dgn-np:NP930126.RARR8S7F-Nc4Oazb-2ivaxIcz_lb7lFotxoLYPTXW8OmA130_provenance
{
dgn-np:NP930126.RARR8S7F-Nc4Oazb-2ivaxIcz_lb7lFotxoLYPTXW8OmA130_assertion
dcterms:description
"[The first human clinical trials of gene therapy for RPE65 associated retinal dystrophy have shown promising initial results and have helped prepare the way for further trials of gene therapy for inherited retinal 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:22080959
;
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:NP930126.RARR8S7F-Nc4Oazb-2ivaxIcz_lb7lFotxoLYPTXW8OmA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:30+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" .
}