@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP241090.RAaoU-ZX4LZraahL0iinLr1PtHP_oNZtt0GRcuvOlpN3Q
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP241090.RAaoU-ZX4LZraahL0iinLr1PtHP_oNZtt0GRcuvOlpN3Q130_assertion
;
np:hasProvenance
dgn-np:NP241090.RAaoU-ZX4LZraahL0iinLr1PtHP_oNZtt0GRcuvOlpN3Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP241090.RAaoU-ZX4LZraahL0iinLr1PtHP_oNZtt0GRcuvOlpN3Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP241090.RAaoU-ZX4LZraahL0iinLr1PtHP_oNZtt0GRcuvOlpN3Q130_assertion
a
np:Assertion
.
dgn-np:NP241090.RAaoU-ZX4LZraahL0iinLr1PtHP_oNZtt0GRcuvOlpN3Q130_provenance
a
np:Provenance
.
dgn-np:NP241090.RAaoU-ZX4LZraahL0iinLr1PtHP_oNZtt0GRcuvOlpN3Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP241090.RAaoU-ZX4LZraahL0iinLr1PtHP_oNZtt0GRcuvOlpN3Q130_assertion
{
miriam-gene:3416
a
ncit:C16612
.
lld:C0011849
a
ncit:C7057
.
dgn-gda:DGNc697783e49a090581f893f791563d88b
sio:SIO_000628
miriam-gene:3416
,
lld:C0011849
;
a
sio:SIO_001121
.
}
dgn-np:NP241090.RAaoU-ZX4LZraahL0iinLr1PtHP_oNZtt0GRcuvOlpN3Q130_provenance
{
dgn-np:NP241090.RAaoU-ZX4LZraahL0iinLr1PtHP_oNZtt0GRcuvOlpN3Q130_assertion
dcterms:description
"[In the absence of convincing support for this association from linkage partitioning or analyses of continuous measures of glycemia, we conclude that analysis of over 2,400 samples provides no compelling evidence that variation in IDE contributes to diabetes susceptibility in humans.]. 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:12716770
;
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:NP241090.RAaoU-ZX4LZraahL0iinLr1PtHP_oNZtt0GRcuvOlpN3Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:15+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" .
}