@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP891485.RA4HnwUIAWo-DT98RzdKDYlgT12j6DCqoohe_3EapvUGY
> .
@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:NP891485.RA4HnwUIAWo-DT98RzdKDYlgT12j6DCqoohe_3EapvUGY130_head
{
this:
np:hasAssertion
dgn-np:NP891485.RA4HnwUIAWo-DT98RzdKDYlgT12j6DCqoohe_3EapvUGY130_assertion
;
np:hasProvenance
dgn-np:NP891485.RA4HnwUIAWo-DT98RzdKDYlgT12j6DCqoohe_3EapvUGY130_provenance
;
np:hasPublicationInfo
dgn-np:NP891485.RA4HnwUIAWo-DT98RzdKDYlgT12j6DCqoohe_3EapvUGY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP891485.RA4HnwUIAWo-DT98RzdKDYlgT12j6DCqoohe_3EapvUGY130_assertion
a
np:Assertion
.
dgn-np:NP891485.RA4HnwUIAWo-DT98RzdKDYlgT12j6DCqoohe_3EapvUGY130_provenance
a
np:Provenance
.
dgn-np:NP891485.RA4HnwUIAWo-DT98RzdKDYlgT12j6DCqoohe_3EapvUGY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP891485.RA4HnwUIAWo-DT98RzdKDYlgT12j6DCqoohe_3EapvUGY130_assertion
{
miriam-gene:7391
a
ncit:C16612
.
lld:C0011847
a
ncit:C7057
.
dgn-gda:DGN56a77f28aa7e762d2657c5364416a9bc
sio:SIO_000628
miriam-gene:7391
,
lld:C0011847
;
a
sio:SIO_001121
.
}
dgn-np:NP891485.RA4HnwUIAWo-DT98RzdKDYlgT12j6DCqoohe_3EapvUGY130_provenance
{
dgn-np:NP891485.RA4HnwUIAWo-DT98RzdKDYlgT12j6DCqoohe_3EapvUGY130_assertion
dcterms:description
"[We genotyped three haplotype-tagging single nucleotide polymorphisms (SNPs) (rs3737787, rs2516841 and rs2516839) at USF1 in three samples of the Hong Kong Chinese population, including members of 179 families from the Hong Kong Family Diabetes Study, 1,383 hospital cases with type 2 diabetes and/or the metabolic syndrome and 454 normal control subjects.]. 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:16132950
;
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:NP891485.RA4HnwUIAWo-DT98RzdKDYlgT12j6DCqoohe_3EapvUGY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:08+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" .
}