@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP829529.RAxgMN3ZGibWJ9MUzpWPpCstZZ1hHutQVXH06diqnioa8
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP829529.RAxgMN3ZGibWJ9MUzpWPpCstZZ1hHutQVXH06diqnioa8130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP829529.RAxgMN3ZGibWJ9MUzpWPpCstZZ1hHutQVXH06diqnioa8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP829529.RAxgMN3ZGibWJ9MUzpWPpCstZZ1hHutQVXH06diqnioa8130_assertion
a
np:Assertion
.
dgn-np:NP829529.RAxgMN3ZGibWJ9MUzpWPpCstZZ1hHutQVXH06diqnioa8130_provenance
a
np:Provenance
.
dgn-np:NP829529.RAxgMN3ZGibWJ9MUzpWPpCstZZ1hHutQVXH06diqnioa8130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:208
a
ncit:C16612
.
lld:C0025517
a
ncit:C7057
.
dgn-gda:DGNcc43ce715d60f47a244ea509e55db0c5
sio:SIO_000628
miriam-gene:208
,
lld:C0025517
;
a
sio:SIO_001121
.
}
dgn-np:NP829529.RAxgMN3ZGibWJ9MUzpWPpCstZZ1hHutQVXH06diqnioa8130_provenance
{
dgn-np:NP829529.RAxgMN3ZGibWJ9MUzpWPpCstZZ1hHutQVXH06diqnioa8130_assertion
dcterms:description
"[To determine whether genetic variation in AKT2 plays a broader role in human metabolic disease, we sequenced the entire coding region and splice junctions of AKT2 in 94 unrelated patients with severe insulin resistance, 35 of whom had partial lipodystrophy.]. 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:17327441
;
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 .
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dgn-np:NP829529.RAxgMN3ZGibWJ9MUzpWPpCstZZ1hHutQVXH06diqnioa8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:27+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
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"v2.1.0" .
}