@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP55817.RAhg6IK5C1rV7fLJUcQbX1HwT9ZovdgOwHDe0rnacwdbs
> .
@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:NP55817.RAhg6IK5C1rV7fLJUcQbX1HwT9ZovdgOwHDe0rnacwdbs130_head
{
this:
np:hasAssertion
dgn-np:NP55817.RAhg6IK5C1rV7fLJUcQbX1HwT9ZovdgOwHDe0rnacwdbs130_assertion
;
np:hasProvenance
dgn-np:NP55817.RAhg6IK5C1rV7fLJUcQbX1HwT9ZovdgOwHDe0rnacwdbs130_provenance
;
np:hasPublicationInfo
dgn-np:NP55817.RAhg6IK5C1rV7fLJUcQbX1HwT9ZovdgOwHDe0rnacwdbs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP55817.RAhg6IK5C1rV7fLJUcQbX1HwT9ZovdgOwHDe0rnacwdbs130_assertion
a
np:Assertion
.
dgn-np:NP55817.RAhg6IK5C1rV7fLJUcQbX1HwT9ZovdgOwHDe0rnacwdbs130_provenance
a
np:Provenance
.
dgn-np:NP55817.RAhg6IK5C1rV7fLJUcQbX1HwT9ZovdgOwHDe0rnacwdbs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP55817.RAhg6IK5C1rV7fLJUcQbX1HwT9ZovdgOwHDe0rnacwdbs130_assertion
{
miriam-gene:3667
a
ncit:C16612
.
lld:C0021655
a
ncit:C7057
.
dgn-gda:DGNd5943b2790dd91d7a362b4226e10db47
sio:SIO_000628
miriam-gene:3667
,
lld:C0021655
;
a
sio:SIO_001122
.
}
dgn-np:NP55817.RAhg6IK5C1rV7fLJUcQbX1HwT9ZovdgOwHDe0rnacwdbs130_provenance
{
dgn-np:NP55817.RAhg6IK5C1rV7fLJUcQbX1HwT9ZovdgOwHDe0rnacwdbs130_assertion
dcterms:description
"[ While subtle effects of these variants cannot be excluded in this system, it is unlikely that these variants are responsible for the extreme insulin resistance seen in the subjects harbouring them. Although IRS proteins play a central role in insulin signalling, functionally significant mutations in the IRS-1 gene are a rare cause of human syndromes of severe insulin resistance.]. 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:12358865
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP55817.RAhg6IK5C1rV7fLJUcQbX1HwT9ZovdgOwHDe0rnacwdbs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:26+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" .
}