@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP584022.RAuqP3iucPedJlpJUcIr0bjSXVnZoKPxwW3opB-rPidyE
> .
@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:NP584022.RAuqP3iucPedJlpJUcIr0bjSXVnZoKPxwW3opB-rPidyE130_head
{
this:
np:hasAssertion
dgn-np:NP584022.RAuqP3iucPedJlpJUcIr0bjSXVnZoKPxwW3opB-rPidyE130_assertion
;
np:hasProvenance
dgn-np:NP584022.RAuqP3iucPedJlpJUcIr0bjSXVnZoKPxwW3opB-rPidyE130_provenance
;
np:hasPublicationInfo
dgn-np:NP584022.RAuqP3iucPedJlpJUcIr0bjSXVnZoKPxwW3opB-rPidyE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP584022.RAuqP3iucPedJlpJUcIr0bjSXVnZoKPxwW3opB-rPidyE130_assertion
a
np:Assertion
.
dgn-np:NP584022.RAuqP3iucPedJlpJUcIr0bjSXVnZoKPxwW3opB-rPidyE130_provenance
a
np:Provenance
.
dgn-np:NP584022.RAuqP3iucPedJlpJUcIr0bjSXVnZoKPxwW3opB-rPidyE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP584022.RAuqP3iucPedJlpJUcIr0bjSXVnZoKPxwW3opB-rPidyE130_assertion
{
miriam-gene:3767
a
ncit:C16612
.
lld:C0342276
a
ncit:C7057
.
dgn-gda:DGN7751f18d3aaf3f20a88f6b213778d8fd
sio:SIO_000628
miriam-gene:3767
,
lld:C0342276
;
a
sio:SIO_001121
.
}
dgn-np:NP584022.RAuqP3iucPedJlpJUcIr0bjSXVnZoKPxwW3opB-rPidyE130_provenance
{
dgn-np:NP584022.RAuqP3iucPedJlpJUcIr0bjSXVnZoKPxwW3opB-rPidyE130_assertion
dcterms:description
"[Finally, the example of single gene diabetes, particularly HNF1A MODY and permanent neonatal diabetes associated with the KCNJ11 and ABCC8 genes, all efficiently controlled on sulfonylurea, inspires us to continue the efforts to tailor individual treatment for T2DM patients.]. 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:22996131
;
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:NP584022.RAuqP3iucPedJlpJUcIr0bjSXVnZoKPxwW3opB-rPidyE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:51+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" .
}