@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP555176.RAn7i2tJtnPPaMWEivIHbPauG0GpQaaDGz-HrqDRBFGsw
> .
@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:NP555176.RAn7i2tJtnPPaMWEivIHbPauG0GpQaaDGz-HrqDRBFGsw130_head
{
this:
np:hasAssertion
dgn-np:NP555176.RAn7i2tJtnPPaMWEivIHbPauG0GpQaaDGz-HrqDRBFGsw130_assertion
;
np:hasProvenance
dgn-np:NP555176.RAn7i2tJtnPPaMWEivIHbPauG0GpQaaDGz-HrqDRBFGsw130_provenance
;
np:hasPublicationInfo
dgn-np:NP555176.RAn7i2tJtnPPaMWEivIHbPauG0GpQaaDGz-HrqDRBFGsw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP555176.RAn7i2tJtnPPaMWEivIHbPauG0GpQaaDGz-HrqDRBFGsw130_assertion
a
np:Assertion
.
dgn-np:NP555176.RAn7i2tJtnPPaMWEivIHbPauG0GpQaaDGz-HrqDRBFGsw130_provenance
a
np:Provenance
.
dgn-np:NP555176.RAn7i2tJtnPPaMWEivIHbPauG0GpQaaDGz-HrqDRBFGsw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP555176.RAn7i2tJtnPPaMWEivIHbPauG0GpQaaDGz-HrqDRBFGsw130_assertion
{
miriam-gene:3767
a
ncit:C16612
.
lld:C0011880
a
ncit:C7057
.
dgn-gda:DGN6f8f98523cf7f560bc5aebb94c0c27c5
sio:SIO_000628
miriam-gene:3767
,
lld:C0011880
;
a
sio:SIO_001121
.
}
dgn-np:NP555176.RAn7i2tJtnPPaMWEivIHbPauG0GpQaaDGz-HrqDRBFGsw130_provenance
{
dgn-np:NP555176.RAn7i2tJtnPPaMWEivIHbPauG0GpQaaDGz-HrqDRBFGsw130_assertion
dcterms:description
"[Comparing the 6q24 abnormality and KCNJ11 mutation, there were some significant clinical differences: the earlier onset of diabetes, the lower frequency of diabetic ketoacidosis at onset, and the higher proportion of the patients with macroglossia at initial presentation in the patients with 6q24 abnormality.]. 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:17635943
;
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:NP555176.RAn7i2tJtnPPaMWEivIHbPauG0GpQaaDGz-HrqDRBFGsw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:34+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" .
}