@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP258786.RAurE_T4eyJeUsDHNEVhpR_uNE8wFUUdHW66ZvMO3C8cg
> .
@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:NP258786.RAurE_T4eyJeUsDHNEVhpR_uNE8wFUUdHW66ZvMO3C8cg130_head
{
this:
np:hasAssertion
dgn-np:NP258786.RAurE_T4eyJeUsDHNEVhpR_uNE8wFUUdHW66ZvMO3C8cg130_assertion
;
np:hasProvenance
dgn-np:NP258786.RAurE_T4eyJeUsDHNEVhpR_uNE8wFUUdHW66ZvMO3C8cg130_provenance
;
np:hasPublicationInfo
dgn-np:NP258786.RAurE_T4eyJeUsDHNEVhpR_uNE8wFUUdHW66ZvMO3C8cg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP258786.RAurE_T4eyJeUsDHNEVhpR_uNE8wFUUdHW66ZvMO3C8cg130_assertion
a
np:Assertion
.
dgn-np:NP258786.RAurE_T4eyJeUsDHNEVhpR_uNE8wFUUdHW66ZvMO3C8cg130_provenance
a
np:Provenance
.
dgn-np:NP258786.RAurE_T4eyJeUsDHNEVhpR_uNE8wFUUdHW66ZvMO3C8cg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP258786.RAurE_T4eyJeUsDHNEVhpR_uNE8wFUUdHW66ZvMO3C8cg130_assertion
{
miriam-gene:3643
a
ncit:C16612
.
lld:C0020459
a
ncit:C7057
.
dgn-gda:DGN1e735d679a69d1446acbd8c783e28b6f
sio:SIO_000628
miriam-gene:3643
,
lld:C0020459
;
a
sio:SIO_001121
.
}
dgn-np:NP258786.RAurE_T4eyJeUsDHNEVhpR_uNE8wFUUdHW66ZvMO3C8cg130_provenance
{
dgn-np:NP258786.RAurE_T4eyJeUsDHNEVhpR_uNE8wFUUdHW66ZvMO3C8cg130_assertion
dcterms:description
"[Because acanthosis nigricans is commonly accompanied by severe hyperinsulinemia and obesity, and obesity is a major factor in insulin resistance, this study was initiated to assess the prevalence of mutations in the insulin receptor gene in Chinese patients with extreme insulin resistance defined by hyperinsulinemia, obesity and acanthosis nigricans.]. 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:9872020
;
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:NP258786.RAurE_T4eyJeUsDHNEVhpR_uNE8wFUUdHW66ZvMO3C8cg130_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" .
}