@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP324668.RATXxW94LKej2C2Qv7IHrkUU7vbfhcLX9qFPKMCf-NN-I
> .
@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:NP324668.RATXxW94LKej2C2Qv7IHrkUU7vbfhcLX9qFPKMCf-NN-I130_head
{
this:
np:hasAssertion
dgn-np:NP324668.RATXxW94LKej2C2Qv7IHrkUU7vbfhcLX9qFPKMCf-NN-I130_assertion
;
np:hasProvenance
dgn-np:NP324668.RATXxW94LKej2C2Qv7IHrkUU7vbfhcLX9qFPKMCf-NN-I130_provenance
;
np:hasPublicationInfo
dgn-np:NP324668.RATXxW94LKej2C2Qv7IHrkUU7vbfhcLX9qFPKMCf-NN-I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP324668.RATXxW94LKej2C2Qv7IHrkUU7vbfhcLX9qFPKMCf-NN-I130_assertion
a
np:Assertion
.
dgn-np:NP324668.RATXxW94LKej2C2Qv7IHrkUU7vbfhcLX9qFPKMCf-NN-I130_provenance
a
np:Provenance
.
dgn-np:NP324668.RATXxW94LKej2C2Qv7IHrkUU7vbfhcLX9qFPKMCf-NN-I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP324668.RATXxW94LKej2C2Qv7IHrkUU7vbfhcLX9qFPKMCf-NN-I130_assertion
{
miriam-gene:3767
a
ncit:C16612
.
lld:C0011849
a
ncit:C7057
.
dgn-gda:DGNce07e38bb40443fcb645827118b8d09d
sio:SIO_000628
miriam-gene:3767
,
lld:C0011849
;
a
sio:SIO_001121
.
}
dgn-np:NP324668.RATXxW94LKej2C2Qv7IHrkUU7vbfhcLX9qFPKMCf-NN-I130_provenance
{
dgn-np:NP324668.RATXxW94LKej2C2Qv7IHrkUU7vbfhcLX9qFPKMCf-NN-I130_assertion
dcterms:description
"[These results broaden the spectrum of diabetes phenotypes caused by mutations of KCNJ11 and suggest that mutations in this gene should be taken into consideration for not only permanent neonatal diabetes but also other forms of diabetes with milder phenotypes and later onset.]. 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:15784703
;
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:NP324668.RATXxW94LKej2C2Qv7IHrkUU7vbfhcLX9qFPKMCf-NN-I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:10+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" .
}