@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP744560.RAkPx26tj1jm5iacTNGcv-mQDEUaxRf172LDc09wED_eo
> .
@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:NP744560.RAkPx26tj1jm5iacTNGcv-mQDEUaxRf172LDc09wED_eo130_head
{
this:
np:hasAssertion
dgn-np:NP744560.RAkPx26tj1jm5iacTNGcv-mQDEUaxRf172LDc09wED_eo130_assertion
;
np:hasProvenance
dgn-np:NP744560.RAkPx26tj1jm5iacTNGcv-mQDEUaxRf172LDc09wED_eo130_provenance
;
np:hasPublicationInfo
dgn-np:NP744560.RAkPx26tj1jm5iacTNGcv-mQDEUaxRf172LDc09wED_eo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP744560.RAkPx26tj1jm5iacTNGcv-mQDEUaxRf172LDc09wED_eo130_assertion
a
np:Assertion
.
dgn-np:NP744560.RAkPx26tj1jm5iacTNGcv-mQDEUaxRf172LDc09wED_eo130_provenance
a
np:Provenance
.
dgn-np:NP744560.RAkPx26tj1jm5iacTNGcv-mQDEUaxRf172LDc09wED_eo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP744560.RAkPx26tj1jm5iacTNGcv-mQDEUaxRf172LDc09wED_eo130_assertion
{
miriam-gene:3030
a
ncit:C16612
.
lld:C0020615
a
ncit:C7057
.
dgn-gda:DGNf07299ae8ed95cd5e368638fc5b3c497
sio:SIO_000628
miriam-gene:3030
,
lld:C0020615
;
a
sio:SIO_001121
.
}
dgn-np:NP744560.RAkPx26tj1jm5iacTNGcv-mQDEUaxRf172LDc09wED_eo130_provenance
{
dgn-np:NP744560.RAkPx26tj1jm5iacTNGcv-mQDEUaxRf172LDc09wED_eo130_assertion
dcterms:description
"[We investigated individuals with hyperinsulinaemic hypoglycaemia and biochemical or genetic evidence to suggest noncoding mutations by using NGS to analyze the entire genomic regions of ABCC8 (117 kb) and HADH (94 kb) from overlapping ~10 kb PCR amplicons.]. 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:23273570
;
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:NP744560.RAkPx26tj1jm5iacTNGcv-mQDEUaxRf172LDc09wED_eo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:31+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" .
}