@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP71422.RAek3oaH8WQj1VpKOFaauuAIhUp736EBIm8GExhxkei_E
> .
@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:NP71422.RAek3oaH8WQj1VpKOFaauuAIhUp736EBIm8GExhxkei_E130_head
{
this:
np:hasAssertion
dgn-np:NP71422.RAek3oaH8WQj1VpKOFaauuAIhUp736EBIm8GExhxkei_E130_assertion
;
np:hasProvenance
dgn-np:NP71422.RAek3oaH8WQj1VpKOFaauuAIhUp736EBIm8GExhxkei_E130_provenance
;
np:hasPublicationInfo
dgn-np:NP71422.RAek3oaH8WQj1VpKOFaauuAIhUp736EBIm8GExhxkei_E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP71422.RAek3oaH8WQj1VpKOFaauuAIhUp736EBIm8GExhxkei_E130_assertion
a
np:Assertion
.
dgn-np:NP71422.RAek3oaH8WQj1VpKOFaauuAIhUp736EBIm8GExhxkei_E130_provenance
a
np:Provenance
.
dgn-np:NP71422.RAek3oaH8WQj1VpKOFaauuAIhUp736EBIm8GExhxkei_E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP71422.RAek3oaH8WQj1VpKOFaauuAIhUp736EBIm8GExhxkei_E130_assertion
{
miriam-gene:3784
a
ncit:C16612
.
lld:C0011860
a
ncit:C7057
.
dgn-gda:DGN70a0e8e8c25e308eec0f24386960f505
sio:SIO_000628
miriam-gene:3784
,
lld:C0011860
;
a
sio:SIO_001122
.
}
dgn-np:NP71422.RAek3oaH8WQj1VpKOFaauuAIhUp736EBIm8GExhxkei_E130_provenance
{
dgn-np:NP71422.RAek3oaH8WQj1VpKOFaauuAIhUp736EBIm8GExhxkei_E130_assertion
dct:description
"[We observed numerous regions with suggestive associations with type 2 diabetes. Some of these signals correspond to regions described in previous studies. However, many of these regions could not be replicated in the DIAGRAM datasets. It is critical to carry out additional studies in Hispanic and American Indian populations, which have a high prevalence of type 2 diabetes.]. 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:21573907
;
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:NP71422.RAek3oaH8WQj1VpKOFaauuAIhUp736EBIm8GExhxkei_E130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:34+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" .
}