@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP450879.RA1-U7XrbdPqRShzV271VkmPwPe4IPKC4zcNsUyJ4T5yQ
> .
@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:NP450879.RA1-U7XrbdPqRShzV271VkmPwPe4IPKC4zcNsUyJ4T5yQ130_head
{
this:
np:hasAssertion
dgn-np:NP450879.RA1-U7XrbdPqRShzV271VkmPwPe4IPKC4zcNsUyJ4T5yQ130_assertion
;
np:hasProvenance
dgn-np:NP450879.RA1-U7XrbdPqRShzV271VkmPwPe4IPKC4zcNsUyJ4T5yQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP450879.RA1-U7XrbdPqRShzV271VkmPwPe4IPKC4zcNsUyJ4T5yQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP450879.RA1-U7XrbdPqRShzV271VkmPwPe4IPKC4zcNsUyJ4T5yQ130_assertion
a
np:Assertion
.
dgn-np:NP450879.RA1-U7XrbdPqRShzV271VkmPwPe4IPKC4zcNsUyJ4T5yQ130_provenance
a
np:Provenance
.
dgn-np:NP450879.RA1-U7XrbdPqRShzV271VkmPwPe4IPKC4zcNsUyJ4T5yQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP450879.RA1-U7XrbdPqRShzV271VkmPwPe4IPKC4zcNsUyJ4T5yQ130_assertion
{
miriam-gene:7263
a
ncit:C16612
.
lld:C1320640
a
ncit:C7057
.
dgn-gda:DGN912be48d29d800605093249aa9f7f20f
sio:SIO_000628
miriam-gene:7263
,
lld:C1320640
;
a
sio:SIO_001121
.
}
dgn-np:NP450879.RA1-U7XrbdPqRShzV271VkmPwPe4IPKC4zcNsUyJ4T5yQ130_provenance
{
dgn-np:NP450879.RA1-U7XrbdPqRShzV271VkmPwPe4IPKC4zcNsUyJ4T5yQ130_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:NP450879.RA1-U7XrbdPqRShzV271VkmPwPe4IPKC4zcNsUyJ4T5yQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:29+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" .
}