@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP665714.RAL2f9ExkRydnWCPxusGwMjHclZFA20LXGvWAYiRZNTv0
> .
@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:NP665714.RAL2f9ExkRydnWCPxusGwMjHclZFA20LXGvWAYiRZNTv0130_head
{
this:
np:hasAssertion
dgn-np:NP665714.RAL2f9ExkRydnWCPxusGwMjHclZFA20LXGvWAYiRZNTv0130_assertion
;
np:hasProvenance
dgn-np:NP665714.RAL2f9ExkRydnWCPxusGwMjHclZFA20LXGvWAYiRZNTv0130_provenance
;
np:hasPublicationInfo
dgn-np:NP665714.RAL2f9ExkRydnWCPxusGwMjHclZFA20LXGvWAYiRZNTv0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP665714.RAL2f9ExkRydnWCPxusGwMjHclZFA20LXGvWAYiRZNTv0130_assertion
a
np:Assertion
.
dgn-np:NP665714.RAL2f9ExkRydnWCPxusGwMjHclZFA20LXGvWAYiRZNTv0130_provenance
a
np:Provenance
.
dgn-np:NP665714.RAL2f9ExkRydnWCPxusGwMjHclZFA20LXGvWAYiRZNTv0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP665714.RAL2f9ExkRydnWCPxusGwMjHclZFA20LXGvWAYiRZNTv0130_assertion
{
miriam-gene:3630
a
ncit:C16612
.
lld:C0265344
a
ncit:C7057
.
dgn-gda:DGN8456f954954f0b933c44ba2a851d58df
sio:SIO_000628
miriam-gene:3630
,
lld:C0265344
;
a
sio:SIO_001121
.
}
dgn-np:NP665714.RAL2f9ExkRydnWCPxusGwMjHclZFA20LXGvWAYiRZNTv0130_provenance
{
dgn-np:NP665714.RAL2f9ExkRydnWCPxusGwMjHclZFA20LXGvWAYiRZNTv0130_assertion
dcterms:description
"[Homozygous or compound heterozygous mutations within the insulin binding domain of the human insulin receptor (INSR) are usually associated with severe impairment of insulin binding leading to Donohue syndrome (Leprechaunism), which is characterized by excessive hyperglycemia with hyperinsulinism, pre- and postnatal growth retardation, distinct dysmorphism and early death.]. 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:18411068
;
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:NP665714.RAL2f9ExkRydnWCPxusGwMjHclZFA20LXGvWAYiRZNTv0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:47+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" .
}