@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP294620.RAu0ik3K4UD9KX2tE3weN161vCMRqIq7yTaXjTNIEmmbY
> .
@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:NP294620.RAu0ik3K4UD9KX2tE3weN161vCMRqIq7yTaXjTNIEmmbY130_head
{
this:
np:hasAssertion
dgn-np:NP294620.RAu0ik3K4UD9KX2tE3weN161vCMRqIq7yTaXjTNIEmmbY130_assertion
;
np:hasProvenance
dgn-np:NP294620.RAu0ik3K4UD9KX2tE3weN161vCMRqIq7yTaXjTNIEmmbY130_provenance
;
np:hasPublicationInfo
dgn-np:NP294620.RAu0ik3K4UD9KX2tE3weN161vCMRqIq7yTaXjTNIEmmbY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP294620.RAu0ik3K4UD9KX2tE3weN161vCMRqIq7yTaXjTNIEmmbY130_assertion
a
np:Assertion
.
dgn-np:NP294620.RAu0ik3K4UD9KX2tE3weN161vCMRqIq7yTaXjTNIEmmbY130_provenance
a
np:Provenance
.
dgn-np:NP294620.RAu0ik3K4UD9KX2tE3weN161vCMRqIq7yTaXjTNIEmmbY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP294620.RAu0ik3K4UD9KX2tE3weN161vCMRqIq7yTaXjTNIEmmbY130_assertion
{
miriam-gene:1636
a
ncit:C16612
.
lld:C0011847
a
ncit:C7057
.
dgn-gda:DGNcc0d51008527bf8806a724b1eaf76dd0
sio:SIO_000628
miriam-gene:1636
,
lld:C0011847
;
a
sio:SIO_001121
.
}
dgn-np:NP294620.RAu0ik3K4UD9KX2tE3weN161vCMRqIq7yTaXjTNIEmmbY130_provenance
{
dgn-np:NP294620.RAu0ik3K4UD9KX2tE3weN161vCMRqIq7yTaXjTNIEmmbY130_assertion
dcterms:description
"[Multiple regression analysis showed that the effect of the ACE genotype was explained by its influence on serum ACE activity and that the only other significant determinants of the risk of severe hypoglycaemia were the degree of hypoglycaemia awareness, b-cell function, and duration of diabetes of more than 20 years.]. 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:11418149
;
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:NP294620.RAu0ik3K4UD9KX2tE3weN161vCMRqIq7yTaXjTNIEmmbY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:47+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" .
}