@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP688130.RATNuDwFXMS2zJIn1UaRBeyUVdhQB52QvG0mpCo5dinnU
> .
@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:NP688130.RATNuDwFXMS2zJIn1UaRBeyUVdhQB52QvG0mpCo5dinnU130_head
{
this:
np:hasAssertion
dgn-np:NP688130.RATNuDwFXMS2zJIn1UaRBeyUVdhQB52QvG0mpCo5dinnU130_assertion
;
np:hasProvenance
dgn-np:NP688130.RATNuDwFXMS2zJIn1UaRBeyUVdhQB52QvG0mpCo5dinnU130_provenance
;
np:hasPublicationInfo
dgn-np:NP688130.RATNuDwFXMS2zJIn1UaRBeyUVdhQB52QvG0mpCo5dinnU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP688130.RATNuDwFXMS2zJIn1UaRBeyUVdhQB52QvG0mpCo5dinnU130_assertion
a
np:Assertion
.
dgn-np:NP688130.RATNuDwFXMS2zJIn1UaRBeyUVdhQB52QvG0mpCo5dinnU130_provenance
a
np:Provenance
.
dgn-np:NP688130.RATNuDwFXMS2zJIn1UaRBeyUVdhQB52QvG0mpCo5dinnU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP688130.RATNuDwFXMS2zJIn1UaRBeyUVdhQB52QvG0mpCo5dinnU130_assertion
{
miriam-gene:217
a
ncit:C16612
.
lld:C0010068
a
ncit:C7057
.
dgn-gda:DGNab00b8a8b3b2c31ce25806b23908fdac
sio:SIO_000628
miriam-gene:217
,
lld:C0010068
;
a
sio:SIO_001121
.
}
dgn-np:NP688130.RATNuDwFXMS2zJIn1UaRBeyUVdhQB52QvG0mpCo5dinnU130_provenance
{
dgn-np:NP688130.RATNuDwFXMS2zJIn1UaRBeyUVdhQB52QvG0mpCo5dinnU130_assertion
dcterms:description
"[These findings suggest that the ALDH2 polymorphism is associated with an increased risk of T2DM in female CAD patients, and this association could be causal on the basis of the association between the polymorphism and FPG, which is partly explained by an increased inflammatory status.]. 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:19876063
;
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:NP688130.RATNuDwFXMS2zJIn1UaRBeyUVdhQB52QvG0mpCo5dinnU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:58+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" .
}