@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP47644.RAX6QAnNei1N0wvVMGCWouD2K7Ips5aR17Wi12rJpOGNQ
> .
@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#
> .
dgn-np:NP47644.RAX6QAnNei1N0wvVMGCWouD2K7Ips5aR17Wi12rJpOGNQ130_head
{
this:
np:hasAssertion
dgn-np:NP47644.RAX6QAnNei1N0wvVMGCWouD2K7Ips5aR17Wi12rJpOGNQ130_assertion
;
np:hasProvenance
dgn-np:NP47644.RAX6QAnNei1N0wvVMGCWouD2K7Ips5aR17Wi12rJpOGNQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP47644.RAX6QAnNei1N0wvVMGCWouD2K7Ips5aR17Wi12rJpOGNQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP47644.RAX6QAnNei1N0wvVMGCWouD2K7Ips5aR17Wi12rJpOGNQ130_assertion
a
np:Assertion
.
dgn-np:NP47644.RAX6QAnNei1N0wvVMGCWouD2K7Ips5aR17Wi12rJpOGNQ130_provenance
a
np:Provenance
.
dgn-np:NP47644.RAX6QAnNei1N0wvVMGCWouD2K7Ips5aR17Wi12rJpOGNQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP47644.RAX6QAnNei1N0wvVMGCWouD2K7Ips5aR17Wi12rJpOGNQ130_assertion
{
miriam-gene:11132
a
ncit:C16612
.
lld:C0011860
a
ncit:C7057
.
dgn-gda:DGN72421873fda076688d24f6996d1694b8
sio:SIO_000628
miriam-gene:11132
,
lld:C0011860
;
a
sio:SIO_001122
.
}
dgn-np:NP47644.RAX6QAnNei1N0wvVMGCWouD2K7Ips5aR17Wi12rJpOGNQ130_provenance
{
dgn-np:NP47644.RAX6QAnNei1N0wvVMGCWouD2K7Ips5aR17Wi12rJpOGNQ130_assertion
dcterms:description
"[The association of the polymorphisms Gly972Arg, SNP43, and Pro12Ala, of the genes IRS1, CAPN10, PPARG2, with the risk of failure to sulphonylurea and metformin therapies was determinated in patients with DT2 in Yucatn, Mxico.]. 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:19418728
;
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:NP47644.RAX6QAnNei1N0wvVMGCWouD2K7Ips5aR17Wi12rJpOGNQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:21+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" .
}