@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1307720.RAtJ0JvofWz0AK1QxBkt3x8Z_ebTki78ku_MIkVKUfbxc
> .
@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:NP1307720.RAtJ0JvofWz0AK1QxBkt3x8Z_ebTki78ku_MIkVKUfbxc130_head
{
this:
np:hasAssertion
dgn-np:NP1307720.RAtJ0JvofWz0AK1QxBkt3x8Z_ebTki78ku_MIkVKUfbxc130_assertion
;
np:hasProvenance
dgn-np:NP1307720.RAtJ0JvofWz0AK1QxBkt3x8Z_ebTki78ku_MIkVKUfbxc130_provenance
;
np:hasPublicationInfo
dgn-np:NP1307720.RAtJ0JvofWz0AK1QxBkt3x8Z_ebTki78ku_MIkVKUfbxc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1307720.RAtJ0JvofWz0AK1QxBkt3x8Z_ebTki78ku_MIkVKUfbxc130_assertion
a
np:Assertion
.
dgn-np:NP1307720.RAtJ0JvofWz0AK1QxBkt3x8Z_ebTki78ku_MIkVKUfbxc130_provenance
a
np:Provenance
.
dgn-np:NP1307720.RAtJ0JvofWz0AK1QxBkt3x8Z_ebTki78ku_MIkVKUfbxc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1307720.RAtJ0JvofWz0AK1QxBkt3x8Z_ebTki78ku_MIkVKUfbxc130_assertion
{
miriam-gene:6652
a
ncit:C16612
.
lld:C0011849
a
ncit:C7057
.
dgn-gda:DGNb427ee5b883e4d233ea313d5b5fcd011
sio:SIO_000628
miriam-gene:6652
,
lld:C0011849
;
a
sio:SIO_001121
.
}
dgn-np:NP1307720.RAtJ0JvofWz0AK1QxBkt3x8Z_ebTki78ku_MIkVKUfbxc130_provenance
{
dgn-np:NP1307720.RAtJ0JvofWz0AK1QxBkt3x8Z_ebTki78ku_MIkVKUfbxc130_assertion
dcterms:description
"[These results do not define a clear cataract-SORD deficiency etiopathogenic relationship, nevertheless, they strongly suggest activity polymorphism in human red cell SORD, which would be highly relevant not only to the study of cataracts but of other major complications in diabetes.]. 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:7152518
;
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:NP1307720.RAtJ0JvofWz0AK1QxBkt3x8Z_ebTki78ku_MIkVKUfbxc130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:38+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" .
}