@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP82858.RA1NJmBzRPMiVMRw69QWKHEgGAiw4tnxSnER-bAvsgKEY
> .
@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:NP82858.RA1NJmBzRPMiVMRw69QWKHEgGAiw4tnxSnER-bAvsgKEY130_head
{
this:
np:hasAssertion
dgn-np:NP82858.RA1NJmBzRPMiVMRw69QWKHEgGAiw4tnxSnER-bAvsgKEY130_assertion
;
np:hasProvenance
dgn-np:NP82858.RA1NJmBzRPMiVMRw69QWKHEgGAiw4tnxSnER-bAvsgKEY130_provenance
;
np:hasPublicationInfo
dgn-np:NP82858.RA1NJmBzRPMiVMRw69QWKHEgGAiw4tnxSnER-bAvsgKEY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP82858.RA1NJmBzRPMiVMRw69QWKHEgGAiw4tnxSnER-bAvsgKEY130_assertion
a
np:Assertion
.
dgn-np:NP82858.RA1NJmBzRPMiVMRw69QWKHEgGAiw4tnxSnER-bAvsgKEY130_provenance
a
np:Provenance
.
dgn-np:NP82858.RA1NJmBzRPMiVMRw69QWKHEgGAiw4tnxSnER-bAvsgKEY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP82858.RA1NJmBzRPMiVMRw69QWKHEgGAiw4tnxSnER-bAvsgKEY130_assertion
{
miriam-gene:5789
a
ncit:C16612
.
lld:C0011860
a
ncit:C7057
.
dgn-gda:DGN3c4fbb197f97127662297a86bf7382a5
sio:SIO_000628
miriam-gene:5789
,
lld:C0011860
;
a
sio:SIO_001122
.
}
dgn-np:NP82858.RA1NJmBzRPMiVMRw69QWKHEgGAiw4tnxSnER-bAvsgKEY130_provenance
{
dgn-np:NP82858.RA1NJmBzRPMiVMRw69QWKHEgGAiw4tnxSnER-bAvsgKEY130_assertion
dct:description
"[In the largest study of type 2 diabetes in Mexican populations to date, we identified modest associations of novel and previously reported SNPs. In addition, in our top signals we report significant excess of SNPs that predict transcript levels in muscle and adipose tissues.]. 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:21647700
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP82858.RA1NJmBzRPMiVMRw69QWKHEgGAiw4tnxSnER-bAvsgKEY130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:40+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" .
}