@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP931876.RA5f-KLOu_JBL39Z_yse6fYbR39rj5KbKaDGD7dhjFIvM
> .
@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:NP931876.RA5f-KLOu_JBL39Z_yse6fYbR39rj5KbKaDGD7dhjFIvM130_head
{
this:
np:hasAssertion
dgn-np:NP931876.RA5f-KLOu_JBL39Z_yse6fYbR39rj5KbKaDGD7dhjFIvM130_assertion
;
np:hasProvenance
dgn-np:NP931876.RA5f-KLOu_JBL39Z_yse6fYbR39rj5KbKaDGD7dhjFIvM130_provenance
;
np:hasPublicationInfo
dgn-np:NP931876.RA5f-KLOu_JBL39Z_yse6fYbR39rj5KbKaDGD7dhjFIvM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP931876.RA5f-KLOu_JBL39Z_yse6fYbR39rj5KbKaDGD7dhjFIvM130_assertion
a
np:Assertion
.
dgn-np:NP931876.RA5f-KLOu_JBL39Z_yse6fYbR39rj5KbKaDGD7dhjFIvM130_provenance
a
np:Provenance
.
dgn-np:NP931876.RA5f-KLOu_JBL39Z_yse6fYbR39rj5KbKaDGD7dhjFIvM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP931876.RA5f-KLOu_JBL39Z_yse6fYbR39rj5KbKaDGD7dhjFIvM130_assertion
{
miriam-gene:5362
a
ncit:C16612
.
lld:C3276549
a
ncit:C7057
.
dgn-gda:DGNe4c481d3f5e6640d07f8507241fa48df
sio:SIO_000628
miriam-gene:5362
,
lld:C3276549
;
a
sio:SIO_001121
.
}
dgn-np:NP931876.RA5f-KLOu_JBL39Z_yse6fYbR39rj5KbKaDGD7dhjFIvM130_provenance
{
dgn-np:NP931876.RA5f-KLOu_JBL39Z_yse6fYbR39rj5KbKaDGD7dhjFIvM130_assertion
dcterms:description
"[In this prospective, observational case series, optical coherence tomography (OCT) was used to define the pattern of retinal nerve fibre layer (RNFL) loss in patients with both the pure and syndromal forms of DOA.]. 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:21378995
;
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:NP931876.RA5f-KLOu_JBL39Z_yse6fYbR39rj5KbKaDGD7dhjFIvM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:31+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" .
}