@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP921860.RA4CSXQ6OYFsG09Dv_ScR_m41Vf3TjENqMFHadNLOyj5Q
> .
@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:NP921860.RA4CSXQ6OYFsG09Dv_ScR_m41Vf3TjENqMFHadNLOyj5Q130_head
{
this:
np:hasAssertion
dgn-np:NP921860.RA4CSXQ6OYFsG09Dv_ScR_m41Vf3TjENqMFHadNLOyj5Q130_assertion
;
np:hasProvenance
dgn-np:NP921860.RA4CSXQ6OYFsG09Dv_ScR_m41Vf3TjENqMFHadNLOyj5Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP921860.RA4CSXQ6OYFsG09Dv_ScR_m41Vf3TjENqMFHadNLOyj5Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP921860.RA4CSXQ6OYFsG09Dv_ScR_m41Vf3TjENqMFHadNLOyj5Q130_assertion
a
np:Assertion
.
dgn-np:NP921860.RA4CSXQ6OYFsG09Dv_ScR_m41Vf3TjENqMFHadNLOyj5Q130_provenance
a
np:Provenance
.
dgn-np:NP921860.RA4CSXQ6OYFsG09Dv_ScR_m41Vf3TjENqMFHadNLOyj5Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP921860.RA4CSXQ6OYFsG09Dv_ScR_m41Vf3TjENqMFHadNLOyj5Q130_assertion
{
miriam-gene:57096
a
ncit:C16612
.
lld:C0035309
a
ncit:C7057
.
dgn-gda:DGNf583b72ecaad0a1ae54fa2fdfdc276ec
sio:SIO_000628
miriam-gene:57096
,
lld:C0035309
;
a
sio:SIO_001121
.
}
dgn-np:NP921860.RA4CSXQ6OYFsG09Dv_ScR_m41Vf3TjENqMFHadNLOyj5Q130_provenance
{
dgn-np:NP921860.RA4CSXQ6OYFsG09Dv_ScR_m41Vf3TjENqMFHadNLOyj5Q130_assertion
dcterms:description
"[In this study, RPGRIP1, RANBP2, NPM1, PDE6D, NPHP5, and ABCA4 genes were selected on the basis of interaction with RPGR or RPGRIP1 or their implication in related retinal diseases, and were investigated as candidate genetic modifiers of XLPRA1.]. 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:17653054
;
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:NP921860.RA4CSXQ6OYFsG09Dv_ScR_m41Vf3TjENqMFHadNLOyj5Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:25+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" .
}