@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP496797.RAvxPzQPfHf2LgfX_PUqH6CDhTZpE8lJprBhm2-DGEv3g
> .
@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:NP496797.RAvxPzQPfHf2LgfX_PUqH6CDhTZpE8lJprBhm2-DGEv3g130_head
{
this:
np:hasAssertion
dgn-np:NP496797.RAvxPzQPfHf2LgfX_PUqH6CDhTZpE8lJprBhm2-DGEv3g130_assertion
;
np:hasProvenance
dgn-np:NP496797.RAvxPzQPfHf2LgfX_PUqH6CDhTZpE8lJprBhm2-DGEv3g130_provenance
;
np:hasPublicationInfo
dgn-np:NP496797.RAvxPzQPfHf2LgfX_PUqH6CDhTZpE8lJprBhm2-DGEv3g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP496797.RAvxPzQPfHf2LgfX_PUqH6CDhTZpE8lJprBhm2-DGEv3g130_assertion
a
np:Assertion
.
dgn-np:NP496797.RAvxPzQPfHf2LgfX_PUqH6CDhTZpE8lJprBhm2-DGEv3g130_provenance
a
np:Provenance
.
dgn-np:NP496797.RAvxPzQPfHf2LgfX_PUqH6CDhTZpE8lJprBhm2-DGEv3g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP496797.RAvxPzQPfHf2LgfX_PUqH6CDhTZpE8lJprBhm2-DGEv3g130_assertion
{
miriam-gene:8431
a
ncit:C16612
.
lld:C0011847
a
ncit:C7057
.
dgn-gda:DGNb87f1c418bf13a35310fa611e158bcf1
sio:SIO_000628
miriam-gene:8431
,
lld:C0011847
;
a
sio:SIO_001121
.
}
dgn-np:NP496797.RAvxPzQPfHf2LgfX_PUqH6CDhTZpE8lJprBhm2-DGEv3g130_provenance
{
dgn-np:NP496797.RAvxPzQPfHf2LgfX_PUqH6CDhTZpE8lJprBhm2-DGEv3g130_assertion
dcterms:description
"[The results suggest that the increases in insulin sensitivity through multiple signaling pathways in muscle, liver, and fat, with an increase in islet secretory function, represent the complex mechanism whereby SHP deficiency leads to improvement in insulin sensitivity, secretion, and diabetes.]. 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:16803864
;
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:NP496797.RAvxPzQPfHf2LgfX_PUqH6CDhTZpE8lJprBhm2-DGEv3g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:56+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" .
}