@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP217848.RABVHU1PheENsgqFSq82ejOiwDY9ulQXaI1ymoprtpuF4
> .
@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:NP217848.RABVHU1PheENsgqFSq82ejOiwDY9ulQXaI1ymoprtpuF4130_head
{
this:
np:hasAssertion
dgn-np:NP217848.RABVHU1PheENsgqFSq82ejOiwDY9ulQXaI1ymoprtpuF4130_assertion
;
np:hasProvenance
dgn-np:NP217848.RABVHU1PheENsgqFSq82ejOiwDY9ulQXaI1ymoprtpuF4130_provenance
;
np:hasPublicationInfo
dgn-np:NP217848.RABVHU1PheENsgqFSq82ejOiwDY9ulQXaI1ymoprtpuF4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP217848.RABVHU1PheENsgqFSq82ejOiwDY9ulQXaI1ymoprtpuF4130_assertion
a
np:Assertion
.
dgn-np:NP217848.RABVHU1PheENsgqFSq82ejOiwDY9ulQXaI1ymoprtpuF4130_provenance
a
np:Provenance
.
dgn-np:NP217848.RABVHU1PheENsgqFSq82ejOiwDY9ulQXaI1ymoprtpuF4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP217848.RABVHU1PheENsgqFSq82ejOiwDY9ulQXaI1ymoprtpuF4130_assertion
{
miriam-gene:5961
a
ncit:C16612
.
lld:C1320640
a
ncit:C7057
.
dgn-gda:DGNe7ed99bd02a5bd90cf8ecbc950a27e72
sio:SIO_000628
miriam-gene:5961
,
lld:C1320640
;
a
sio:SIO_001121
.
}
dgn-np:NP217848.RABVHU1PheENsgqFSq82ejOiwDY9ulQXaI1ymoprtpuF4130_provenance
{
dgn-np:NP217848.RABVHU1PheENsgqFSq82ejOiwDY9ulQXaI1ymoprtpuF4130_assertion
dcterms:description
"[The RDS gene has been implicated in the mouse phenotype retinal degeneration slow, and mutations in the human homologue are now known to be associated with both central and peripheral retinal degenerations.]. 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:8956033
;
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:NP217848.RABVHU1PheENsgqFSq82ejOiwDY9ulQXaI1ymoprtpuF4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:01+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" .
}