@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP493827.RAUl5N6L1XgRJDd1umDTwNkQ_XkJ7C813od3cDUA2rCOE
> .
@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:NP493827.RAUl5N6L1XgRJDd1umDTwNkQ_XkJ7C813od3cDUA2rCOE130_head
{
this:
np:hasAssertion
dgn-np:NP493827.RAUl5N6L1XgRJDd1umDTwNkQ_XkJ7C813od3cDUA2rCOE130_assertion
;
np:hasProvenance
dgn-np:NP493827.RAUl5N6L1XgRJDd1umDTwNkQ_XkJ7C813od3cDUA2rCOE130_provenance
;
np:hasPublicationInfo
dgn-np:NP493827.RAUl5N6L1XgRJDd1umDTwNkQ_XkJ7C813od3cDUA2rCOE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP493827.RAUl5N6L1XgRJDd1umDTwNkQ_XkJ7C813od3cDUA2rCOE130_assertion
a
np:Assertion
.
dgn-np:NP493827.RAUl5N6L1XgRJDd1umDTwNkQ_XkJ7C813od3cDUA2rCOE130_provenance
a
np:Provenance
.
dgn-np:NP493827.RAUl5N6L1XgRJDd1umDTwNkQ_XkJ7C813od3cDUA2rCOE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP493827.RAUl5N6L1XgRJDd1umDTwNkQ_XkJ7C813od3cDUA2rCOE130_assertion
{
miriam-gene:115861
a
ncit:C16612
.
lld:C0035334
a
ncit:C7057
.
dgn-gda:DGN2d9c9056c2cc18e1ed6be869b69ac8d4
sio:SIO_000628
miriam-gene:115861
,
lld:C0035334
;
a
sio:SIO_001121
.
}
dgn-np:NP493827.RAUl5N6L1XgRJDd1umDTwNkQ_XkJ7C813od3cDUA2rCOE130_provenance
{
dgn-np:NP493827.RAUl5N6L1XgRJDd1umDTwNkQ_XkJ7C813od3cDUA2rCOE130_assertion
dcterms:description
"[The demonstration at the functional level of the therapeutic potential of RdCVF in the most frequent of dominant RP mutations paves the way toward the use of RdCVF for preserving central vision in many RP patients.]. 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:19277021
;
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:NP493827.RAUl5N6L1XgRJDd1umDTwNkQ_XkJ7C813od3cDUA2rCOE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:55+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" .
}