@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP880531.RAFMIk2LkmOc5QvT8XNDlL8Ysn82fbJsYx9QSMRdoXzYA
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP880531.RAFMIk2LkmOc5QvT8XNDlL8Ysn82fbJsYx9QSMRdoXzYA130_head
{
this:
np:hasAssertion
dgn-np:NP880531.RAFMIk2LkmOc5QvT8XNDlL8Ysn82fbJsYx9QSMRdoXzYA130_assertion
;
np:hasProvenance
dgn-np:NP880531.RAFMIk2LkmOc5QvT8XNDlL8Ysn82fbJsYx9QSMRdoXzYA130_provenance
;
np:hasPublicationInfo
dgn-np:NP880531.RAFMIk2LkmOc5QvT8XNDlL8Ysn82fbJsYx9QSMRdoXzYA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP880531.RAFMIk2LkmOc5QvT8XNDlL8Ysn82fbJsYx9QSMRdoXzYA130_assertion
a
np:Assertion
.
dgn-np:NP880531.RAFMIk2LkmOc5QvT8XNDlL8Ysn82fbJsYx9QSMRdoXzYA130_provenance
a
np:Provenance
.
dgn-np:NP880531.RAFMIk2LkmOc5QvT8XNDlL8Ysn82fbJsYx9QSMRdoXzYA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP880531.RAFMIk2LkmOc5QvT8XNDlL8Ysn82fbJsYx9QSMRdoXzYA130_assertion
{
miriam-gene:25970
a
ncit:C16612
.
lld:C0011860
a
ncit:C7057
.
dgn-gda:DGN7489c47334b881418f34f58d508771eb
sio:SIO_000628
miriam-gene:25970
,
lld:C0011860
;
a
sio:SIO_001122
.
}
dgn-np:NP880531.RAFMIk2LkmOc5QvT8XNDlL8Ysn82fbJsYx9QSMRdoXzYA130_provenance
{
dgn-np:NP880531.RAFMIk2LkmOc5QvT8XNDlL8Ysn82fbJsYx9QSMRdoXzYA130_assertion
dcterms:description
"[The SH2B1 tag SNP rs4788102 (SNP, single nucleotide polymorphism) was genotyped in 6978 individuals from six studies for abnormal glucose homeostasis (AGH), including impaired fasting glucose, impaired glucose tolerance or T2D, from the GENetics of Type 2 Diabetes in Italy and the United States (GENIUS T2D) consortium.]. 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:24103803
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP880531.RAFMIk2LkmOc5QvT8XNDlL8Ysn82fbJsYx9QSMRdoXzYA130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:46:36+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}