@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP176784.RA2eXjlff4acOocSZ9e_6W69l6XW_LAYe4UNPA93cOvRI
> .
@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:NP176784.RA2eXjlff4acOocSZ9e_6W69l6XW_LAYe4UNPA93cOvRI130_head
{
this:
np:hasAssertion
dgn-np:NP176784.RA2eXjlff4acOocSZ9e_6W69l6XW_LAYe4UNPA93cOvRI130_assertion
;
np:hasProvenance
dgn-np:NP176784.RA2eXjlff4acOocSZ9e_6W69l6XW_LAYe4UNPA93cOvRI130_provenance
;
np:hasPublicationInfo
dgn-np:NP176784.RA2eXjlff4acOocSZ9e_6W69l6XW_LAYe4UNPA93cOvRI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP176784.RA2eXjlff4acOocSZ9e_6W69l6XW_LAYe4UNPA93cOvRI130_assertion
a
np:Assertion
.
dgn-np:NP176784.RA2eXjlff4acOocSZ9e_6W69l6XW_LAYe4UNPA93cOvRI130_provenance
a
np:Provenance
.
dgn-np:NP176784.RA2eXjlff4acOocSZ9e_6W69l6XW_LAYe4UNPA93cOvRI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP176784.RA2eXjlff4acOocSZ9e_6W69l6XW_LAYe4UNPA93cOvRI130_assertion
{
miriam-gene:2645
a
ncit:C16612
.
lld:C0011860
a
ncit:C7057
.
dgn-gda:DGN7b4fc59cf790148eb344e40c7be049a3
sio:SIO_000628
miriam-gene:2645
,
lld:C0011860
;
a
sio:SIO_001121
.
}
dgn-np:NP176784.RA2eXjlff4acOocSZ9e_6W69l6XW_LAYe4UNPA93cOvRI130_provenance
{
dgn-np:NP176784.RA2eXjlff4acOocSZ9e_6W69l6XW_LAYe4UNPA93cOvRI130_assertion
dcterms:description
"[Thus, it is possible that impairment in the regulation of glucokinase gene expression or its enzyme activity is associated with at least some Japanese NIDDM patients, though the prevalence of the mutations in the coding region is relatively low.]. 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:7859592
;
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:NP176784.RA2eXjlff4acOocSZ9e_6W69l6XW_LAYe4UNPA93cOvRI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:35+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" .
}