@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP671331.RAxjiOte5cSG3bSb3wmzdE_T19Hf9sHCc4WO35aNlDj2c
> .
@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:NP671331.RAxjiOte5cSG3bSb3wmzdE_T19Hf9sHCc4WO35aNlDj2c130_head
{
this:
np:hasAssertion
dgn-np:NP671331.RAxjiOte5cSG3bSb3wmzdE_T19Hf9sHCc4WO35aNlDj2c130_assertion
;
np:hasProvenance
dgn-np:NP671331.RAxjiOte5cSG3bSb3wmzdE_T19Hf9sHCc4WO35aNlDj2c130_provenance
;
np:hasPublicationInfo
dgn-np:NP671331.RAxjiOte5cSG3bSb3wmzdE_T19Hf9sHCc4WO35aNlDj2c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP671331.RAxjiOte5cSG3bSb3wmzdE_T19Hf9sHCc4WO35aNlDj2c130_assertion
a
np:Assertion
.
dgn-np:NP671331.RAxjiOte5cSG3bSb3wmzdE_T19Hf9sHCc4WO35aNlDj2c130_provenance
a
np:Provenance
.
dgn-np:NP671331.RAxjiOte5cSG3bSb3wmzdE_T19Hf9sHCc4WO35aNlDj2c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP671331.RAxjiOte5cSG3bSb3wmzdE_T19Hf9sHCc4WO35aNlDj2c130_assertion
{
miriam-gene:9451
a
ncit:C16612
.
lld:C0011847
a
ncit:C7057
.
dgn-gda:DGN4ccda6adbd5b3565923cb4573bbda84f
sio:SIO_000628
miriam-gene:9451
,
lld:C0011847
;
a
sio:SIO_001121
.
}
dgn-np:NP671331.RAxjiOte5cSG3bSb3wmzdE_T19Hf9sHCc4WO35aNlDj2c130_provenance
{
dgn-np:NP671331.RAxjiOte5cSG3bSb3wmzdE_T19Hf9sHCc4WO35aNlDj2c130_assertion
dcterms:description
"[Remarkably, the onset of diabetes was relatively late (30 months) in the patient expressing the partially defective EIF2AK3 mutant and in the patient with no EIF2AK3 involvement (18 months) compared with other patients (<6 months).]. 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:15220213
;
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:NP671331.RAxjiOte5cSG3bSb3wmzdE_T19Hf9sHCc4WO35aNlDj2c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:45+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" .
}