@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP675867.RAwDZQ4qjABNUPDPBgvJ8_KNb1MhnaTBv_aixnhGdipFc
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP675867.RAwDZQ4qjABNUPDPBgvJ8_KNb1MhnaTBv_aixnhGdipFc130_head
{
this:
np:hasAssertion
dgn-np:NP675867.RAwDZQ4qjABNUPDPBgvJ8_KNb1MhnaTBv_aixnhGdipFc130_assertion
;
np:hasProvenance
dgn-np:NP675867.RAwDZQ4qjABNUPDPBgvJ8_KNb1MhnaTBv_aixnhGdipFc130_provenance
;
np:hasPublicationInfo
dgn-np:NP675867.RAwDZQ4qjABNUPDPBgvJ8_KNb1MhnaTBv_aixnhGdipFc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP675867.RAwDZQ4qjABNUPDPBgvJ8_KNb1MhnaTBv_aixnhGdipFc130_assertion
a
np:Assertion
.
dgn-np:NP675867.RAwDZQ4qjABNUPDPBgvJ8_KNb1MhnaTBv_aixnhGdipFc130_provenance
a
np:Provenance
.
dgn-np:NP675867.RAwDZQ4qjABNUPDPBgvJ8_KNb1MhnaTBv_aixnhGdipFc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP675867.RAwDZQ4qjABNUPDPBgvJ8_KNb1MhnaTBv_aixnhGdipFc130_assertion
{
miriam-gene:3767
a
ncit:C16612
.
lld:C0158981
a
ncit:C7057
.
dgn-gda:DGN10335c28aa967c6537718da84490f6d5
sio:SIO_000628
miriam-gene:3767
,
lld:C0158981
;
a
sio:SIO_001121
.
}
dgn-np:NP675867.RAwDZQ4qjABNUPDPBgvJ8_KNb1MhnaTBv_aixnhGdipFc130_provenance
{
dgn-np:NP675867.RAwDZQ4qjABNUPDPBgvJ8_KNb1MhnaTBv_aixnhGdipFc130_assertion
dcterms:description
"[They indicate testing for KCNJ11 mutations should be considered not only for neonatal diabetes but also for other forms of dominantly inherited diabetes with later onset, especially where these are associated with a low body mass index and low birth weight.]. 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:18544102
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP675867.RAwDZQ4qjABNUPDPBgvJ8_KNb1MhnaTBv_aixnhGdipFc130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:51+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}