@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP68844.RAPYQyIpq59oDLQA8q5KXGl-0N99TrGn6pEbLBK67o8MQ
> .
@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:NP68844.RAPYQyIpq59oDLQA8q5KXGl-0N99TrGn6pEbLBK67o8MQ130_head
{
this:
np:hasAssertion
dgn-np:NP68844.RAPYQyIpq59oDLQA8q5KXGl-0N99TrGn6pEbLBK67o8MQ130_assertion
;
np:hasProvenance
dgn-np:NP68844.RAPYQyIpq59oDLQA8q5KXGl-0N99TrGn6pEbLBK67o8MQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP68844.RAPYQyIpq59oDLQA8q5KXGl-0N99TrGn6pEbLBK67o8MQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP68844.RAPYQyIpq59oDLQA8q5KXGl-0N99TrGn6pEbLBK67o8MQ130_assertion
a
np:Assertion
.
dgn-np:NP68844.RAPYQyIpq59oDLQA8q5KXGl-0N99TrGn6pEbLBK67o8MQ130_provenance
a
np:Provenance
.
dgn-np:NP68844.RAPYQyIpq59oDLQA8q5KXGl-0N99TrGn6pEbLBK67o8MQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP68844.RAPYQyIpq59oDLQA8q5KXGl-0N99TrGn6pEbLBK67o8MQ130_assertion
{
miriam-gene:10891
a
ncit:C16612
.
lld:C0021655
a
ncit:C7057
.
dgn-gda:DGN9dbcee43a11a19a5791e582486b1dcf0
sio:SIO_000628
miriam-gene:10891
,
lld:C0021655
;
a
sio:SIO_001122
.
}
dgn-np:NP68844.RAPYQyIpq59oDLQA8q5KXGl-0N99TrGn6pEbLBK67o8MQ130_provenance
{
dgn-np:NP68844.RAPYQyIpq59oDLQA8q5KXGl-0N99TrGn6pEbLBK67o8MQ130_assertion
dcterms:description
"[We confirm an association of the P12A variant in traits commonly ascribed to the insulin resistance syndrome, but not with direct measures of insulin sensitivity. The tendency for this variant to act in a recessive manner with effects on multiple traits m]. 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:11158005
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP68844.RAPYQyIpq59oDLQA8q5KXGl-0N99TrGn6pEbLBK67o8MQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:42:19+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" .
}