@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP356655.RADXBB41PiYR6RAU7Qhlsop0JOTdYI7bCo3WlB-iZ4yac
> .
@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 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:NP356655.RADXBB41PiYR6RAU7Qhlsop0JOTdYI7bCo3WlB-iZ4yac130_head
{
this:
np:hasAssertion
dgn-np:NP356655.RADXBB41PiYR6RAU7Qhlsop0JOTdYI7bCo3WlB-iZ4yac130_assertion
;
np:hasProvenance
dgn-np:NP356655.RADXBB41PiYR6RAU7Qhlsop0JOTdYI7bCo3WlB-iZ4yac130_provenance
;
np:hasPublicationInfo
dgn-np:NP356655.RADXBB41PiYR6RAU7Qhlsop0JOTdYI7bCo3WlB-iZ4yac130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP356655.RADXBB41PiYR6RAU7Qhlsop0JOTdYI7bCo3WlB-iZ4yac130_assertion
a
np:Assertion
.
dgn-np:NP356655.RADXBB41PiYR6RAU7Qhlsop0JOTdYI7bCo3WlB-iZ4yac130_provenance
a
np:Provenance
.
dgn-np:NP356655.RADXBB41PiYR6RAU7Qhlsop0JOTdYI7bCo3WlB-iZ4yac130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP356655.RADXBB41PiYR6RAU7Qhlsop0JOTdYI7bCo3WlB-iZ4yac130_assertion
{
miriam-gene:3133
a
ncit:C16612
.
lld:C0011860
a
ncit:C7057
.
dgn-gda:DGN3a9463a3d741d1031f49877345666337
sio:SIO_000628
miriam-gene:3133
,
lld:C0011860
;
a
sio:SIO_001121
.
}
dgn-np:NP356655.RADXBB41PiYR6RAU7Qhlsop0JOTdYI7bCo3WlB-iZ4yac130_provenance
{
dgn-np:NP356655.RADXBB41PiYR6RAU7Qhlsop0JOTdYI7bCo3WlB-iZ4yac130_assertion
dct:description
"[Because the pathogenesis of retinopathy is likely to be the same in IDDM and NIDDM, NIDDM subjects with retinopathy would be the ideal population to study for an association with MHC markers.]. 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:9157089
;
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:NP356655.RADXBB41PiYR6RAU7Qhlsop0JOTdYI7bCo3WlB-iZ4yac130_publicationInfo
{
this:
dct:created
"2014-10-02T12:35:29+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}