@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP127422.RAdu-TocUfRjKAEnRjVZKZ3FV2sGMMxorlEtyPUiD-Fq8
> .
@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/v3.0.0/void/
> .
dgn-np:NP127422.RAdu-TocUfRjKAEnRjVZKZ3FV2sGMMxorlEtyPUiD-Fq8130_head
{
this:
np:hasAssertion
dgn-np:NP127422.RAdu-TocUfRjKAEnRjVZKZ3FV2sGMMxorlEtyPUiD-Fq8130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP127422.RAdu-TocUfRjKAEnRjVZKZ3FV2sGMMxorlEtyPUiD-Fq8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP127422.RAdu-TocUfRjKAEnRjVZKZ3FV2sGMMxorlEtyPUiD-Fq8130_assertion
a
np:Assertion
.
dgn-np:NP127422.RAdu-TocUfRjKAEnRjVZKZ3FV2sGMMxorlEtyPUiD-Fq8130_provenance
a
np:Provenance
.
dgn-np:NP127422.RAdu-TocUfRjKAEnRjVZKZ3FV2sGMMxorlEtyPUiD-Fq8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP127422.RAdu-TocUfRjKAEnRjVZKZ3FV2sGMMxorlEtyPUiD-Fq8130_assertion
{
miriam-gene:5915
a
ncit:C16612
.
lld:C0027092
a
ncit:C7057
.
dgn-gda:DGNd8e02b7ed1c2a3b22cb13f0c2d72eeed
sio:SIO_000628
miriam-gene:5915
,
lld:C0027092
;
a
sio:SIO_001122
.
}
dgn-np:NP127422.RAdu-TocUfRjKAEnRjVZKZ3FV2sGMMxorlEtyPUiD-Fq8130_provenance
{
dgn-np:NP127422.RAdu-TocUfRjKAEnRjVZKZ3FV2sGMMxorlEtyPUiD-Fq8130_assertion
dcterms:description
"[Five SNP variants in RARbeta were detected in Chinese subjects with high myopia, none of them were associated significantly with high myopia. Further studies are needed to identify which genes are responsible for high myopia.]. 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:20508731
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP127422.RAdu-TocUfRjKAEnRjVZKZ3FV2sGMMxorlEtyPUiD-Fq8130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:51+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
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;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}