@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP20261.RABVNTHTWDOhZPKTP16NS7pQaVRtN-N2JsMoExHc3WJ1o
> .
@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:NP20261.RABVNTHTWDOhZPKTP16NS7pQaVRtN-N2JsMoExHc3WJ1o130_head
{
this:
np:hasAssertion
dgn-np:NP20261.RABVNTHTWDOhZPKTP16NS7pQaVRtN-N2JsMoExHc3WJ1o130_assertion
;
np:hasProvenance
dgn-np:NP20261.RABVNTHTWDOhZPKTP16NS7pQaVRtN-N2JsMoExHc3WJ1o130_provenance
;
np:hasPublicationInfo
dgn-np:NP20261.RABVNTHTWDOhZPKTP16NS7pQaVRtN-N2JsMoExHc3WJ1o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP20261.RABVNTHTWDOhZPKTP16NS7pQaVRtN-N2JsMoExHc3WJ1o130_assertion
a
np:Assertion
.
dgn-np:NP20261.RABVNTHTWDOhZPKTP16NS7pQaVRtN-N2JsMoExHc3WJ1o130_provenance
a
np:Provenance
.
dgn-np:NP20261.RABVNTHTWDOhZPKTP16NS7pQaVRtN-N2JsMoExHc3WJ1o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP20261.RABVNTHTWDOhZPKTP16NS7pQaVRtN-N2JsMoExHc3WJ1o130_assertion
{
miriam-gene:3630
a
ncit:C16612
.
lld:C0011860
a
ncit:C7057
.
dgn-gda:DGNc38a0f4f92637d0e836e999df2dc7aba
sio:SIO_000628
miriam-gene:3630
,
lld:C0011860
;
a
sio:SIO_001121
.
}
dgn-np:NP20261.RABVNTHTWDOhZPKTP16NS7pQaVRtN-N2JsMoExHc3WJ1o130_provenance
{
dgn-np:NP20261.RABVNTHTWDOhZPKTP16NS7pQaVRtN-N2JsMoExHc3WJ1o130_assertion
dcterms:description
"[Single nucleotide polymorphisms (SNPs) in the calpain-10 gene (CAPN-10), which encodes a protein involved in the secretion and action of insulin, and chronic exposure to inorganic arsenic (iAs) through drinking water have been independently associated with an increase in the risk for T2DM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_curated
;
sio:SIO_000772
miriam-pubmed:23349674
;
prov:wasDerivedFrom
dgn-void:ctd_human-20130708
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:ctd_human-20130708
pav:importedOn
"2013-07-24"^^
xsd:date
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
}
dgn-np:NP20261.RABVNTHTWDOhZPKTP16NS7pQaVRtN-N2JsMoExHc3WJ1o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:07+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
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" .
}