@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP474188.RAxNzGKpiWpJMfP4wVLGeOtiaa9w3sMNLtHyIVLGHNEFE
> .
@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:NP474188.RAxNzGKpiWpJMfP4wVLGeOtiaa9w3sMNLtHyIVLGHNEFE130_head
{
this:
np:hasAssertion
dgn-np:NP474188.RAxNzGKpiWpJMfP4wVLGeOtiaa9w3sMNLtHyIVLGHNEFE130_assertion
;
np:hasProvenance
dgn-np:NP474188.RAxNzGKpiWpJMfP4wVLGeOtiaa9w3sMNLtHyIVLGHNEFE130_provenance
;
np:hasPublicationInfo
dgn-np:NP474188.RAxNzGKpiWpJMfP4wVLGeOtiaa9w3sMNLtHyIVLGHNEFE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP474188.RAxNzGKpiWpJMfP4wVLGeOtiaa9w3sMNLtHyIVLGHNEFE130_assertion
a
np:Assertion
.
dgn-np:NP474188.RAxNzGKpiWpJMfP4wVLGeOtiaa9w3sMNLtHyIVLGHNEFE130_provenance
a
np:Provenance
.
dgn-np:NP474188.RAxNzGKpiWpJMfP4wVLGeOtiaa9w3sMNLtHyIVLGHNEFE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP474188.RAxNzGKpiWpJMfP4wVLGeOtiaa9w3sMNLtHyIVLGHNEFE130_assertion
{
miriam-gene:5295
a
ncit:C16612
.
lld:C0342335
a
ncit:C7057
.
dgn-gda:DGN0eeda7e3b0b32ce3599f61e393f76a9b
sio:SIO_000628
miriam-gene:5295
,
lld:C0342335
;
a
sio:SIO_001121
.
}
dgn-np:NP474188.RAxNzGKpiWpJMfP4wVLGeOtiaa9w3sMNLtHyIVLGHNEFE130_provenance
{
dgn-np:NP474188.RAxNzGKpiWpJMfP4wVLGeOtiaa9w3sMNLtHyIVLGHNEFE130_assertion
dcterms:description
"[Our findings extend the genetic causes of severe insulin-resistance syndromes and provide important information with respect to the function of PIK3R1 in normal development and its role in human diseases, including growth delay, Rieger anomaly and other ocular affections, insulin resistance, diabetes, paucity of fat, and ovarian cysts.]. 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:23810378
;
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:NP474188.RAxNzGKpiWpJMfP4wVLGeOtiaa9w3sMNLtHyIVLGHNEFE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:44+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" .
}