@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP828598.RAUxcXzemxuibcMz6MTze5t2dIUd_rsE7FaCHKC1Iwdz8
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP828598.RAUxcXzemxuibcMz6MTze5t2dIUd_rsE7FaCHKC1Iwdz8130_head
{
this:
np:hasAssertion
dgn-np:NP828598.RAUxcXzemxuibcMz6MTze5t2dIUd_rsE7FaCHKC1Iwdz8130_assertion
;
np:hasProvenance
dgn-np:NP828598.RAUxcXzemxuibcMz6MTze5t2dIUd_rsE7FaCHKC1Iwdz8130_provenance
;
np:hasPublicationInfo
dgn-np:NP828598.RAUxcXzemxuibcMz6MTze5t2dIUd_rsE7FaCHKC1Iwdz8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP828598.RAUxcXzemxuibcMz6MTze5t2dIUd_rsE7FaCHKC1Iwdz8130_assertion
a
np:Assertion
.
dgn-np:NP828598.RAUxcXzemxuibcMz6MTze5t2dIUd_rsE7FaCHKC1Iwdz8130_provenance
a
np:Provenance
.
dgn-np:NP828598.RAUxcXzemxuibcMz6MTze5t2dIUd_rsE7FaCHKC1Iwdz8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP828598.RAUxcXzemxuibcMz6MTze5t2dIUd_rsE7FaCHKC1Iwdz8130_assertion
{
miriam-gene:24
a
ncit:C16612
.
lld:C0035304
a
ncit:C7057
.
dgn-gda:DGNc59c9a39369ef6e9f270ac14052c332c
sio:SIO_000628
miriam-gene:24
,
lld:C0035304
;
a
sio:SIO_001121
.
}
dgn-np:NP828598.RAUxcXzemxuibcMz6MTze5t2dIUd_rsE7FaCHKC1Iwdz8130_provenance
{
dgn-np:NP828598.RAUxcXzemxuibcMz6MTze5t2dIUd_rsE7FaCHKC1Iwdz8130_assertion
dcterms:description
"[As orthologous genes are commonly mutated in canine models of human blinding disorders, canine ABCA4 appears to be an ideal candidate gene to identify and study sequence changes in dogs affected by various forms of inherited retinal degeneration.]. 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:20661590
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP828598.RAUxcXzemxuibcMz6MTze5t2dIUd_rsE7FaCHKC1Iwdz8130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:00+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}