@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP585629.RAhax7oOVpUmpLfzKwPXBfh-l-KBKKckZaJ2gQ9dgsQDc
> .
@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:NP585629.RAhax7oOVpUmpLfzKwPXBfh-l-KBKKckZaJ2gQ9dgsQDc130_head
{
this:
np:hasAssertion
dgn-np:NP585629.RAhax7oOVpUmpLfzKwPXBfh-l-KBKKckZaJ2gQ9dgsQDc130_assertion
;
np:hasProvenance
dgn-np:NP585629.RAhax7oOVpUmpLfzKwPXBfh-l-KBKKckZaJ2gQ9dgsQDc130_provenance
;
np:hasPublicationInfo
dgn-np:NP585629.RAhax7oOVpUmpLfzKwPXBfh-l-KBKKckZaJ2gQ9dgsQDc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP585629.RAhax7oOVpUmpLfzKwPXBfh-l-KBKKckZaJ2gQ9dgsQDc130_assertion
a
np:Assertion
.
dgn-np:NP585629.RAhax7oOVpUmpLfzKwPXBfh-l-KBKKckZaJ2gQ9dgsQDc130_provenance
a
np:Provenance
.
dgn-np:NP585629.RAhax7oOVpUmpLfzKwPXBfh-l-KBKKckZaJ2gQ9dgsQDc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP585629.RAhax7oOVpUmpLfzKwPXBfh-l-KBKKckZaJ2gQ9dgsQDc130_assertion
{
miriam-gene:1734
a
ncit:C16612
.
lld:C2931689
a
ncit:C7057
.
dgn-gda:DGNcc9ea6cd4f507cf262a623c8d24aea84
sio:SIO_000628
miriam-gene:1734
,
lld:C2931689
;
a
sio:SIO_001121
.
}
dgn-np:NP585629.RAhax7oOVpUmpLfzKwPXBfh-l-KBKKckZaJ2gQ9dgsQDc130_provenance
{
dgn-np:NP585629.RAhax7oOVpUmpLfzKwPXBfh-l-KBKKckZaJ2gQ9dgsQDc130_assertion
dcterms:description
"[Additionally, systematic review and meta-analysis of the literature for genetic association studies of D2 Thr92Ala polymorphism and DM2 were performed in Medline, Embase, LiLacs, and SciELO, and major meeting databases using the terms 'rs225014' odds ratio (OR) 'thr92ala' OR 'T92A' OR 'dio2 a/g'.]. 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:20566590
;
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:NP585629.RAhax7oOVpUmpLfzKwPXBfh-l-KBKKckZaJ2gQ9dgsQDc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:52+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" .
}