@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP703425.RACDvw9d0y87d6ffz8KOOUvXuxwOnJSYRMVId40Cy2zVE
> .
@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:NP703425.RACDvw9d0y87d6ffz8KOOUvXuxwOnJSYRMVId40Cy2zVE130_head
{
this:
np:hasAssertion
dgn-np:NP703425.RACDvw9d0y87d6ffz8KOOUvXuxwOnJSYRMVId40Cy2zVE130_assertion
;
np:hasProvenance
dgn-np:NP703425.RACDvw9d0y87d6ffz8KOOUvXuxwOnJSYRMVId40Cy2zVE130_provenance
;
np:hasPublicationInfo
dgn-np:NP703425.RACDvw9d0y87d6ffz8KOOUvXuxwOnJSYRMVId40Cy2zVE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP703425.RACDvw9d0y87d6ffz8KOOUvXuxwOnJSYRMVId40Cy2zVE130_assertion
a
np:Assertion
.
dgn-np:NP703425.RACDvw9d0y87d6ffz8KOOUvXuxwOnJSYRMVId40Cy2zVE130_provenance
a
np:Provenance
.
dgn-np:NP703425.RACDvw9d0y87d6ffz8KOOUvXuxwOnJSYRMVId40Cy2zVE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP703425.RACDvw9d0y87d6ffz8KOOUvXuxwOnJSYRMVId40Cy2zVE130_assertion
{
miriam-gene:5158
a
ncit:C16612
.
lld:C0035334
a
ncit:C7057
.
dgn-gda:DGN24969da551dfbd973b87ee0b737eb597
sio:SIO_000628
miriam-gene:5158
,
lld:C0035334
;
a
sio:SIO_001121
.
}
dgn-np:NP703425.RACDvw9d0y87d6ffz8KOOUvXuxwOnJSYRMVId40Cy2zVE130_provenance
{
dgn-np:NP703425.RACDvw9d0y87d6ffz8KOOUvXuxwOnJSYRMVId40Cy2zVE130_assertion
dcterms:description
"[Mutations in PDE6A and the PDE6B genes lead to autosomal recessive (ar) forms of retinitis pigmentosa (RP) in human and to the homologous disease in dogs, designated generalised progressive retinal atrophy (gPRA).]. 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:10782214
;
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:NP703425.RACDvw9d0y87d6ffz8KOOUvXuxwOnJSYRMVId40Cy2zVE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:07+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" .
}