@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP353386.RApsNUPjMyrjzslmKq-JHnFxDXhj-H_lw16qRW6WaUAAo
> .
@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:NP353386.RApsNUPjMyrjzslmKq-JHnFxDXhj-H_lw16qRW6WaUAAo130_head
{
this:
np:hasAssertion
dgn-np:NP353386.RApsNUPjMyrjzslmKq-JHnFxDXhj-H_lw16qRW6WaUAAo130_assertion
;
np:hasProvenance
dgn-np:NP353386.RApsNUPjMyrjzslmKq-JHnFxDXhj-H_lw16qRW6WaUAAo130_provenance
;
np:hasPublicationInfo
dgn-np:NP353386.RApsNUPjMyrjzslmKq-JHnFxDXhj-H_lw16qRW6WaUAAo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP353386.RApsNUPjMyrjzslmKq-JHnFxDXhj-H_lw16qRW6WaUAAo130_assertion
a
np:Assertion
.
dgn-np:NP353386.RApsNUPjMyrjzslmKq-JHnFxDXhj-H_lw16qRW6WaUAAo130_provenance
a
np:Provenance
.
dgn-np:NP353386.RApsNUPjMyrjzslmKq-JHnFxDXhj-H_lw16qRW6WaUAAo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP353386.RApsNUPjMyrjzslmKq-JHnFxDXhj-H_lw16qRW6WaUAAo130_assertion
{
miriam-gene:723961
a
ncit:C16612
.
lld:C0032460
a
ncit:C7057
.
dgn-gda:DGNb533e72a8b7b94956cd8b5745c7856c7
sio:SIO_000628
miriam-gene:723961
,
lld:C0032460
;
a
sio:SIO_001121
.
}
dgn-np:NP353386.RApsNUPjMyrjzslmKq-JHnFxDXhj-H_lw16qRW6WaUAAo130_provenance
{
dgn-np:NP353386.RApsNUPjMyrjzslmKq-JHnFxDXhj-H_lw16qRW6WaUAAo130_assertion
dcterms:description
"[Therefore, several polymorphisms of the genes encoding for the insulin (INS), insulin receptor (INSR) or insulin receptor substrates (IRS) involved in postreceptor signaling have been explored for their association with abnormal sensitivity to insulin in PCOS.]. 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:23697264
;
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:NP353386.RApsNUPjMyrjzslmKq-JHnFxDXhj-H_lw16qRW6WaUAAo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:27+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
pav:version
"v2.1.0" .
}