@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP353043.RAj3UOYAmVMwgUcHsrSgPq5dqWVAt1yn-MW6JKsTy6-bY
> .
@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:NP353043.RAj3UOYAmVMwgUcHsrSgPq5dqWVAt1yn-MW6JKsTy6-bY130_assertion
;
np:hasProvenance
dgn-np:NP353043.RAj3UOYAmVMwgUcHsrSgPq5dqWVAt1yn-MW6JKsTy6-bY130_provenance
;
np:hasPublicationInfo
dgn-np:NP353043.RAj3UOYAmVMwgUcHsrSgPq5dqWVAt1yn-MW6JKsTy6-bY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP353043.RAj3UOYAmVMwgUcHsrSgPq5dqWVAt1yn-MW6JKsTy6-bY130_assertion
a
np:Assertion
.
dgn-np:NP353043.RAj3UOYAmVMwgUcHsrSgPq5dqWVAt1yn-MW6JKsTy6-bY130_provenance
a
np:Provenance
.
dgn-np:NP353043.RAj3UOYAmVMwgUcHsrSgPq5dqWVAt1yn-MW6JKsTy6-bY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP353043.RAj3UOYAmVMwgUcHsrSgPq5dqWVAt1yn-MW6JKsTy6-bY130_assertion
{
miriam-gene:8462
a
ncit:C16612
.
lld:C0011860
a
ncit:C7057
.
dgn-gda:DGNa05d47a30823e1185f6e2287af69b366
sio:SIO_000628
miriam-gene:8462
,
lld:C0011860
;
a
sio:SIO_001121
.
}
dgn-np:NP353043.RAj3UOYAmVMwgUcHsrSgPq5dqWVAt1yn-MW6JKsTy6-bY130_provenance
{
dgn-np:NP353043.RAj3UOYAmVMwgUcHsrSgPq5dqWVAt1yn-MW6JKsTy6-bY130_assertion
dcterms:description
"[The expression of SMAD7 is affected by KLF11, which contains gene variants that have previously been shown to be involved in genetic susceptibility to T2D, and by the highly homologous KLF10.]. 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:17931948
;
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:NP353043.RAj3UOYAmVMwgUcHsrSgPq5dqWVAt1yn-MW6JKsTy6-bY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:27+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" .
}