@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP538262.RAnQRf640Ej7VFvnL2vAaiz_Yd0CaGH9oyo9nIrgc5rZ4
> .
@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:NP538262.RAnQRf640Ej7VFvnL2vAaiz_Yd0CaGH9oyo9nIrgc5rZ4130_head
{
this:
np:hasAssertion
dgn-np:NP538262.RAnQRf640Ej7VFvnL2vAaiz_Yd0CaGH9oyo9nIrgc5rZ4130_assertion
;
np:hasProvenance
dgn-np:NP538262.RAnQRf640Ej7VFvnL2vAaiz_Yd0CaGH9oyo9nIrgc5rZ4130_provenance
;
np:hasPublicationInfo
dgn-np:NP538262.RAnQRf640Ej7VFvnL2vAaiz_Yd0CaGH9oyo9nIrgc5rZ4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP538262.RAnQRf640Ej7VFvnL2vAaiz_Yd0CaGH9oyo9nIrgc5rZ4130_assertion
a
np:Assertion
.
dgn-np:NP538262.RAnQRf640Ej7VFvnL2vAaiz_Yd0CaGH9oyo9nIrgc5rZ4130_provenance
a
np:Provenance
.
dgn-np:NP538262.RAnQRf640Ej7VFvnL2vAaiz_Yd0CaGH9oyo9nIrgc5rZ4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP538262.RAnQRf640Ej7VFvnL2vAaiz_Yd0CaGH9oyo9nIrgc5rZ4130_assertion
{
miriam-gene:3630
a
ncit:C16612
.
lld:C0029928
a
ncit:C7057
.
dgn-gda:DGNf5847b6ac689b05c03e9b96cc138fdf7
sio:SIO_000628
miriam-gene:3630
,
lld:C0029928
;
a
sio:SIO_001121
.
}
dgn-np:NP538262.RAnQRf640Ej7VFvnL2vAaiz_Yd0CaGH9oyo9nIrgc5rZ4130_provenance
{
dgn-np:NP538262.RAnQRf640Ej7VFvnL2vAaiz_Yd0CaGH9oyo9nIrgc5rZ4130_assertion
dcterms:description
"[We concluded that the novel T/C SNP at codon Cys1008 of INSR is associated with decreased insulin sensitivity in Chinese women with PCOS and that the association is not by the change of synthesis or secretion of INSR beta-subunit, but most possibly by the effects of this novel SNP on the function of INSR beta-subunit.]. 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:16510536
;
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:NP538262.RAnQRf640Ej7VFvnL2vAaiz_Yd0CaGH9oyo9nIrgc5rZ4130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:48+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" .
}