@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP754365.RAxYgvOpREJhztQIa9fISQeCtlSDu6nHRhfisTj0ZBD6Q
> .
@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:NP754365.RAxYgvOpREJhztQIa9fISQeCtlSDu6nHRhfisTj0ZBD6Q130_head
{
this:
np:hasAssertion
dgn-np:NP754365.RAxYgvOpREJhztQIa9fISQeCtlSDu6nHRhfisTj0ZBD6Q130_assertion
;
np:hasProvenance
dgn-np:NP754365.RAxYgvOpREJhztQIa9fISQeCtlSDu6nHRhfisTj0ZBD6Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP754365.RAxYgvOpREJhztQIa9fISQeCtlSDu6nHRhfisTj0ZBD6Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP754365.RAxYgvOpREJhztQIa9fISQeCtlSDu6nHRhfisTj0ZBD6Q130_assertion
a
np:Assertion
.
dgn-np:NP754365.RAxYgvOpREJhztQIa9fISQeCtlSDu6nHRhfisTj0ZBD6Q130_provenance
a
np:Provenance
.
dgn-np:NP754365.RAxYgvOpREJhztQIa9fISQeCtlSDu6nHRhfisTj0ZBD6Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP754365.RAxYgvOpREJhztQIa9fISQeCtlSDu6nHRhfisTj0ZBD6Q130_assertion
{
miriam-gene:3630
a
ncit:C16612
.
lld:C0038454
a
ncit:C7057
.
dgn-gda:DGNae2008eabd599c8215dbc005342af7a8
sio:SIO_000628
miriam-gene:3630
,
lld:C0038454
;
a
sio:SIO_001121
.
}
dgn-np:NP754365.RAxYgvOpREJhztQIa9fISQeCtlSDu6nHRhfisTj0ZBD6Q130_provenance
{
dgn-np:NP754365.RAxYgvOpREJhztQIa9fISQeCtlSDu6nHRhfisTj0ZBD6Q130_assertion
dcterms:description
"[Taken together, we suggest that the mtDNA 16189 variant is a predisposing genetic factor for the development of insulin resistance and may be related to various phenotypic expressions in adult life such as development of DM and vascular pathologies involved in stroke and cardiovascular diseases.]. 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:15126308
;
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:NP754365.RAxYgvOpREJhztQIa9fISQeCtlSDu6nHRhfisTj0ZBD6Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:37+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" .
}