@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP258391.RAcLZ4TyMUoVwTfVWv9qAVy_FHWd20myXnvyNM2ftYOvc
> .
@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:NP258391.RAcLZ4TyMUoVwTfVWv9qAVy_FHWd20myXnvyNM2ftYOvc130_head
{
this:
np:hasAssertion
dgn-np:NP258391.RAcLZ4TyMUoVwTfVWv9qAVy_FHWd20myXnvyNM2ftYOvc130_assertion
;
np:hasProvenance
dgn-np:NP258391.RAcLZ4TyMUoVwTfVWv9qAVy_FHWd20myXnvyNM2ftYOvc130_provenance
;
np:hasPublicationInfo
dgn-np:NP258391.RAcLZ4TyMUoVwTfVWv9qAVy_FHWd20myXnvyNM2ftYOvc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP258391.RAcLZ4TyMUoVwTfVWv9qAVy_FHWd20myXnvyNM2ftYOvc130_assertion
a
np:Assertion
.
dgn-np:NP258391.RAcLZ4TyMUoVwTfVWv9qAVy_FHWd20myXnvyNM2ftYOvc130_provenance
a
np:Provenance
.
dgn-np:NP258391.RAcLZ4TyMUoVwTfVWv9qAVy_FHWd20myXnvyNM2ftYOvc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP258391.RAcLZ4TyMUoVwTfVWv9qAVy_FHWd20myXnvyNM2ftYOvc130_assertion
{
miriam-gene:3630
a
ncit:C16612
.
lld:C1280433
a
ncit:C7057
.
dgn-gda:DGN4b7f8571600e9a65dad77424240a224c
sio:SIO_000628
miriam-gene:3630
,
lld:C1280433
;
a
sio:SIO_001121
.
}
dgn-np:NP258391.RAcLZ4TyMUoVwTfVWv9qAVy_FHWd20myXnvyNM2ftYOvc130_provenance
{
dgn-np:NP258391.RAcLZ4TyMUoVwTfVWv9qAVy_FHWd20myXnvyNM2ftYOvc130_assertion
dcterms:description
"[Syndrome of extreme insulin resistance (SEIR) is a rare spectrum disorder with a primary defect in insulin receptor signalling, noted primarily in children, and is often difficult to diagnose due to the clinical heterogeneity.SEIR was diagnosed in an adolescent girl with facial dysmorphism,exuberant scalp and body hair, severe acanthosis, lipoatrophy, dental abnormalities, and short stature (Rabson-Mendenhall phenotype).]. 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:23367497
;
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:NP258391.RAcLZ4TyMUoVwTfVWv9qAVy_FHWd20myXnvyNM2ftYOvc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:24+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" .
}